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 |