The following data is part of a premarket notification filed by Byron Medical with the FDA for Serene Wrap.
| Device ID | K895865 |
| 510k Number | K895865 |
| Device Name: | SERENE WRAP |
| Classification | Gauze/sponge, Internal |
| Applicant | BYRON MEDICAL 3280 E. HEMISPHERE LOOP SUITE 100 Tucson, AZ 85706 |
| Contact | Byron Economidy |
| Correspondent | Byron Economidy BYRON MEDICAL 3280 E. HEMISPHERE LOOP SUITE 100 Tucson, AZ 85706 |
| 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 | 1989-10-02 |
| Decision Date | 1989-12-27 |