510(k) K912347 ยท FYD Apparatus, Exhaust, Surgical
BIPURE 1000
| Applicant | Laser Engineering, Inc., Milford MA, US |
| Decision | Substantially Equivalent, Sep 23, 1991 |
| Received | May 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912347
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.