written by reader A Quick Reference Guide to Official Forms ie 10k, SI, W4BEN etc

by alanh | July 19, 2015 11:51 am

Various posts to our threads often refer to some official form ie 10k S1, W4BEN etc. The aim of this blog is to list each with a brief Plain English explanation of its main purpose and uses, so Gummaratti can quickly get a handle on each. if you post info, please make each post specific to just one form. Also, only post replies if adding specific info or a correction or we will end up with an alphabet soup of info and not be able to find anything (pls dont add ’thanks’ messages, just tick the like button). You may find more detailed info here or elsewher on the net. http://www.investopedia.com/slide-show/sec_filings/[1]
Natch the list wont be sequential, but using CtrlF should help find what you want.

Endnotes:
  1. http://www.investopedia.com/slide-show/sec_filings/: http://www.investopedia.com/slide-show/sec_filings/

Source URL: https://www.stockgumshoe.com/2015/07/microblog-a-quick-reference-guide-to-official-forms-ie-10k-si-w4ben-etc/


7 responses to “written by reader A Quick Reference Guide to Official Forms ie 10k, SI, W4BEN etc”

  1. alanh says:

    Please remember: Post as often as you like, but only about one form per post or the list will become unweildy. The format should be….
    W4BEN: This form tells you about….. xxxxxx. Its main uses are yyyyyyyy. You can also establish zzzzzz from it.

  2. alanh says:

    510k: Overview

    Section 510(k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to market a medical device at least 90 days in advance. This is known as Premarket Notification – also called PMN or 510(k). This allows FDA to determine whether the device is equivalent to a device already placed into one of the three classification categories. Thus, “new” devices (not in commercial distribution prior to May 28, 1976) that have not been classified can be properly identified. Specifically, medical device manufacturers are required to submit a premarket notification if they intend to introduce a device into commercial distribution for the first time or reintroduce a device that will be significantly changed or modified to the extent that its safety or effectiveness could be affected. Such change or modification could relate to the design, material, chemical composition, energy source, manufacturing process, or intended use.

    Listings of CDRH Substantially Equivalent 510(k)s are normally available about the 5th of each month for the prior month. See the links on the left side of this page to find monthly listings of 510(k)s cleared by FDA.
    https://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/DeviceApprovalsandClearances/510kClearances/default.htm

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