510(k) K873521 ยท CAF Nebulizer (Direct Patient Interface)
BRONCHODILATOR TEE - 9056 SERIES
| Applicant | Boehringer Laboratories, Norristown PA, US |
| Decision | Substantially Equivalent, Mar 2, 1988 |
| Received | Sep 1, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873521
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.