510(k) K833633 ยท BSY Catheters, Suction, Tracheobronchial
BRONCHITRAC DF DUAL RESP/CATHETER
| Applicant | Ackrad Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1983 |
| Received | Oct 17, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833633
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.