510(k) K120040 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
REPROCESSED SURGICAL ELECTRIC INSTRUMENT
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 5, 2012 |
| Received | Jan 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120040
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.