The following data is part of a premarket notification filed by Snyder Laboratories, Inc. with the FDA for Snyder Hemovac Wound Drainage Devices.
| Device ID | K843906 |
| 510k Number | K843906 |
| Device Name: | SNYDER HEMOVAC WOUND DRAINAGE DEVICES |
| Classification | Catheter, Ventricular, General & Plastic Surgery |
| Applicant | SNYDER LABORATORIES, INC. P.O. BOX 409 New Philadelphia , OH 44663 - |
| Contact | Kenneth A Hofacker |
| Correspondent | Kenneth A Hofacker SNYDER LABORATORIES, INC. P.O. BOX 409 New Philadelphia , OH 44663 - |
| Product Code | GBS |
| CFR Regulation Number | 878.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-03 |
| Decision Date | 1984-11-05 |