The following data is part of a premarket notification filed by Steven Frank Mercereau with the FDA for Vacvent.
| Device ID | K931873 |
| 510k Number | K931873 |
| Device Name: | VACVENT |
| Classification | Arterial Blood Sampling Kit |
| Applicant | STEVEN FRANK MERCEREAU 4911 WEST LAKE DR. Conyers, GA 30208 |
| Contact | Steven F Mercereau |
| Correspondent | Steven F Mercereau STEVEN FRANK MERCEREAU 4911 WEST LAKE DR. Conyers, GA 30208 |
| Product Code | CBT |
| CFR Regulation Number | 868.1100 [🔎] |
| Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-04-14 |
| Decision Date | 1993-12-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VACVENT 78669025 3170097 Dead/Cancelled |
Jenkins, Bradley E. 2005-07-12 |