510(k) K980522 ยท HQR Apparatus, Cautery, Radiofrequency, Ac-Powered
REFRACTEC MCS-100
| Applicant | Refractec, Inc., Laguna Hills CA, US |
| Decision | Unknown, Jul 22, 1998 |
| Received | Feb 10, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980522
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.