The following data is part of a premarket notification filed by Britt Corp., Inc. with the FDA for Vaso Press Dvt Foot Garment #vp 520.
Device ID | K003828 |
510k Number | K003828 |
Device Name: | VASO PRESS DVT FOOT GARMENT #VP 520 |
Classification | Sleeve, Limb, Compressible |
Applicant | BRITT CORP., INC. 16 CREST DR. Colts Neck, NJ 07722 |
Contact | J J Britton |
Correspondent | J J 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 | 2000-12-11 |
Decision Date | 2001-05-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
40815245010770 | K003828 | 000 |
40815245010725 | K003828 | 000 |
40815245010671 | K003828 | 000 |
40815245010626 | K003828 | 000 |
40815245010572 | K003828 | 000 |