510(k) K945592 ยท FMF Syringe, Piston
VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE
| Applicant | Vlv Associates, Inc., East Hanover NJ, US |
| Decision | Substantially Equivalent, Jul 14, 1995 |
| Received | Nov 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945592
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.