PERIFORM
Perineometer
VERIMED HOLDINGS, INC.
The following data is part of a premarket notification filed by Verimed Holdings, Inc. with the FDA for Periform.
Pre-market Notification Details
| Device ID | K981277 |
| 510k Number | K981277 |
| Device Name: | PERIFORM |
| Classification | Perineometer |
| Applicant | VERIMED HOLDINGS, INC. 11950 N.W. 39TH ST., SUITE D Coral Springs, FL 33065 |
| Contact | Kishore Puppala |
| Correspondent | Kishore Puppala VERIMED HOLDINGS, INC. 11950 N.W. 39TH ST., SUITE D Coral Springs, FL 33065 |
| Product Code | HIR |
| CFR Regulation Number | 884.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-04-08 |
| Decision Date | 1998-11-20 |
| Summary: | summary |
Trademark Results [PERIFORM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERIFORM 75636545 2380728 Dead/Cancelled |
NEEN DESIGN LIMITED 1999-02-09 |
 PERIFORM 72153104 0752918 Dead/Expired |
NATIONAL BROACH AND MACHINE CO. 1962-09-13 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.