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 |