The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Perineometer.
Device ID | K960311 |
510k Number | K960311 |
Device Name: | PERINEOMETER |
Classification | Perineometer |
Applicant | HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
Contact | Joseph S Tokarz |
Correspondent | Joseph S Tokarz HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
Product Code | HIR |
CFR Regulation Number | 884.1425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-22 |
Decision Date | 1996-04-18 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PERINEOMETER 71537323 0546429 Dead/Expired |
KEGEL, ARNOLD H. 1947-10-09 |