510(k) K920209 ยท FYD Apparatus, Exhaust, Surgical
CRF CHARCOAL CANISTER REPLACEMENT FILTER
| Applicant | Quinn Healthcare Products, Washington DC, US |
| Decision | Substantially Equivalent, Oct 1, 1992 |
| Received | Jan 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920209
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.