The following data is part of a premarket notification filed by Carrington Laboratories, Inc. with the FDA for Carrington Wound Dressing.
| Device ID | K902345 |
| 510k Number | K902345 |
| Device Name: | CARRINGTON WOUND DRESSING |
| Classification | Dressing, Wound, Drug |
| Applicant | CARRINGTON LABORATORIES, INC. POST BOX 569003 Dallas, TX 75356 |
| Contact | Bill H Mcanalley |
| Correspondent | Bill H Mcanalley CARRINGTON LABORATORIES, INC. POST BOX 569003 Dallas, TX 75356 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-05-25 |
| Decision Date | 1990-06-07 |