510(k) K920819 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
ABDOVAC (TM), BELLOVAC (TM) AND EXUDRAIN
| Applicant | Astra Meditec AB, Sweden, SE |
| Decision | Unknown, Mar 24, 1993 |
| Received | Feb 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920819
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.