The following data is part of a premarket notification filed by Moss Medical Products with the FDA for Moss - Anchor Set.
Device ID | K913701 |
510k Number | K913701 |
Device Name: | MOSS - ANCHOR SET |
Classification | Tube, Feeding |
Applicant | MOSS MEDICAL PRODUCTS ATTORNEY AT LAW 277 BROADWAY, SUITE 100 New York, NY 10007 |
Contact | Harry A Schlakman |
Correspondent | Harry A Schlakman MOSS MEDICAL PRODUCTS ATTORNEY AT LAW 277 BROADWAY, SUITE 100 New York, NY 10007 |
Product Code | FPD |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-19 |
Decision Date | 1992-02-14 |