The following data is part of a premarket notification filed by Britt Corp., Inc. with the FDA for Vaso Press System.
| Device ID | K974393 |
| 510k Number | K974393 |
| Device Name: | VASO PRESS SYSTEM |
| Classification | Sleeve, Limb, Compressible |
| Applicant | BRITT CORP., INC. PO BOX 547 Freehold, NJ 07728 |
| Contact | J. James Britton |
| Correspondent | J. James Britton BRITT CORP., INC. PO BOX 547 Freehold, NJ 07728 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-11-21 |
| Decision Date | 1999-03-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30815067043874 | K974393 | 000 |
| 30815067043867 | K974393 | 000 |
| 30815067043850 | K974393 | 000 |
| 30815067043843 | K974393 | 000 |
| 30815067043836 | K974393 | 000 |
| 30815067043829 | K974393 | 000 |
| 30815067043430 | K974393 | 000 |
| 30815067043423 | K974393 | 000 |