The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Hollister Retracted Penis Pouch.
| Device ID | K970443 |
| 510k Number | K970443 |
| Device Name: | HOLLISTER RETRACTED PENIS POUCH |
| Classification | Device, Paste-on For Incontinence, Sterile |
| 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 | EXI |
| CFR Regulation Number | 876.5250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-02-05 |
| Decision Date | 1997-02-25 |
| Summary: | summary |