The following data is part of a premarket notification filed by Puricore Inc. with the FDA for Modification To:vashe Wound Cleansing System, Model 9000-0014.
| Device ID | K092232 |
| 510k Number | K092232 |
| Device Name: | MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014 |
| Classification | Dressing, Wound, Drug |
| Applicant | PURICORE INC. 508 LAPP RD. Malvern, PA 19355 |
| Contact | Dennis J Mahoney |
| Correspondent | Dennis J Mahoney PURICORE INC. 508 LAPP RD. Malvern, PA 19355 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | Yes |
| Date Received | 2009-07-23 |
| Decision Date | 2009-08-19 |
| Summary: | summary |