510(k) K920629 ยท FYD Apparatus, Exhaust, Surgical
QUINEVAC II
| Applicant | Recto Molded Products, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 24, 1993 |
| Received | Feb 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920629
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.