510(k) K120898 ยท OTJ Laparoscopic Single Port Access Device
KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CA
| Applicant | Richard Wolf Medical Instruments Corp., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Aug 3, 2012 |
| Received | Mar 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120898
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.