510(k) K062159 ยท FCK Instrument, Biopsy, Suction
RB12 SUCTION RECTAL BIOPSY SYSTEM
| Applicant | Aus Systems Pty , Ltd., Clearwater FL, US |
| Decision | Substantially Equivalent, Sep 5, 2006 |
| Received | Jul 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062159
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.