MEDIFIX
Manometer, Blood-pressure, Venous
BURRON MEDICAL PRODUCTS, INC.
The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Medifix.
Pre-market Notification Details
| Device ID | K813498 |
| 510k Number | K813498 |
| Device Name: | MEDIFIX |
| Classification | Manometer, Blood-pressure, Venous |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KRK |
| CFR Regulation Number | 870.1140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-14 |
| Decision Date | 1982-01-07 |
Trademark Results [MEDIFIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MEDIFIX 85661949 4337584 Dead/Cancelled |
Scapa Group plc 2012-06-26 |
 MEDIFIX 75872904 2519296 Dead/Cancelled |
Medifix Adhesive Products Limited 1999-12-17 |
 MEDIFIX 75207546 2121507 Dead/Cancelled |
MediFix, Inc. 1996-12-03 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.