510(k) K791182 ยท FGA Kit, Nephroscope
ACMI RIGI-FLEX NEPHORSCOPE
| Applicant | American Cystocope Makers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 30, 1979 |
| Received | Jun 25, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791182
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.