The following data is part of a premarket notification filed by Verimed Holdings, Inc. with the FDA for Periform.
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 |
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 |