510(k) K013731 ยท EOQ Bronchoscope (Flexible Or Rigid)
GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03
| Applicant | Gimmi GmbH, Amsterdam, Nh, NL |
| Decision | Substantially Equivalent, Nov 27, 2001 |
| Received | Nov 9, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013731
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.