510(k) K123096 ยท NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
REPROCESSED VESSEL SEALER
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jan 25, 2013 |
| Received | Oct 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123096
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.