The following data is part of a premarket notification filed by E.m. Adams with the FDA for Wet Pack.
| Device ID | K843783 |
| 510k Number | K843783 |
| Device Name: | WET PACK |
| Classification | Gauze/sponge, Internal |
| Applicant | E.M. ADAMS 121 WEST ST. Medfield, MA 02052 |
| Contact | Richard K Donahue |
| Correspondent | Richard K Donahue E.M. ADAMS 121 WEST ST. Medfield, MA 02052 |
| Product Code | EFQ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-26 |
| Decision Date | 1984-12-19 |