The following data is part of a premarket notification filed by Britt Corp., Inc. with the FDA for Vaso Press Dvt System, Models Vp500, Vp501.
| Device ID | K991038 |
| 510k Number | K991038 |
| Device Name: | VASO PRESS DVT SYSTEM, MODELS VP500, VP501 |
| Classification | Sleeve, Limb, Compressible |
| Applicant | BRITT CORP., INC. 16 CREST DR. Colts Neck, NJ 07722 |
| Contact | J. James Britton |
| Correspondent | J. James Britton BRITT CORP., INC. 16 CREST DR. Colts Neck, NJ 07722 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-29 |
| Decision Date | 2000-06-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40815245011814 | K991038 | 000 |
| 40815245011760 | K991038 | 000 |
| 40815245011715 | K991038 | 000 |
| 40815245011661 | K991038 | 000 |
| 40815245011616 | K991038 | 000 |
| 40815245011562 | K991038 | 000 |
| 40815245011517 | K991038 | 000 |
| 40815245011463 | K991038 | 000 |
| 40815245011418 | K991038 | 000 |