The following data is part of a premarket notification filed by Acrymed, Inc. with the FDA for Acryderm Silver Antimicrobial Perforated Wound Dressing.
| Device ID | K012116 |
| 510k Number | K012116 |
| Device Name: | ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING |
| Classification | Dressing, Wound, Drug |
| Applicant | ACRYMED, INC. 12232 S.W. GARDEN PL. Portland, OR 97223 |
| Contact | Bruce Gibbins |
| Correspondent | Bruce Gibbins ACRYMED, INC. 12232 S.W. GARDEN PL. Portland, OR 97223 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-07-06 |
| Decision Date | 2001-09-12 |
| Summary: | summary |