510(k) K952151 ยท HQR Apparatus, Cautery, Radiofrequency, Ac-Powered
STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)
| Applicant | Storz, St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 4, 1996 |
| Received | May 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952151
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.