PERINEOMETER
Perineometer
HOLLISTER, INC.
The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Perineometer.
Pre-market Notification Details
| 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 |
Trademark Results [PERINEOMETER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERINEOMETER 71537323 0546429 Dead/Expired |
KEGEL, ARNOLD H. 1947-10-09 |
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