The following data is part of a premarket notification filed by Gam Industries, Inc. with the FDA for Foil Baby Bunting.
Device ID | K915303 |
510k Number | K915303 |
Device Name: | FOIL BABY BUNTING |
Classification | Bedding, Disposable, Medical |
Applicant | GAM INDUSTRIES, INC. P.O. BOX 2226 Petersburg, VA 23804 -1526 |
Contact | Gary J Beden |
Correspondent | Gary J Beden GAM INDUSTRIES, INC. P.O. BOX 2226 Petersburg, VA 23804 -1526 |
Product Code | KME |
CFR Regulation Number | 880.6060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-11-21 |
Decision Date | 1992-02-20 |