510(k) K912042 ยท LZB Finger Cot
BETHEL PLUS MULTIPLE NAMES
| Applicant | Bethel Latex Products, Inc., Haz;Ejirst MS, US |
| Decision | Substantially Equivalent, Jul 2, 1991 |
| Received | May 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912042
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.