The following data is part of a premarket notification filed by B. Braun Medical, Inc. with the FDA for Prontosan Antimicrobial Wound Gel.
| Device ID | K090141 |
| 510k Number | K090141 |
| Device Name: | PRONTOSAN ANTIMICROBIAL WOUND GEL |
| Classification | Dressing, Wound, Drug |
| Applicant | B. BRAUN MEDICAL, INC. 901 MARCON BLVD. Allentown, PA 18109 -9341 |
| Contact | Lisa Giaquinto |
| Correspondent | Lisa Giaquinto B. BRAUN MEDICAL, INC. 901 MARCON BLVD. Allentown, PA 18109 -9341 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | Yes |
| Date Received | 2009-01-21 |
| Decision Date | 2009-03-17 |
| Summary: | summary |