510(k) K962900 ยท EXJ Device, Incontinence, Urosheath Type, Sterile
SELF RETAINING MALE EXTERNAL URINARY CATHETER
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Sep 16, 1996 |
| Received | Jul 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962900
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.