The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Hollister Female Urinary Collection Pouch.
Device ID | K862934 |
510k Number | K862934 |
Device Name: | HOLLISTER FEMALE URINARY COLLECTION POUCH |
Classification | Collector, Urine, (and Accessories) For Indwelling Catheter |
Applicant | HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
Contact | Jerome A Saxon |
Correspondent | Jerome A Saxon HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
Product Code | KNX |
CFR Regulation Number | 876.5250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-08-04 |
Decision Date | 1986-08-19 |