510(k) K022879 ยท KNW Instrument, Biopsy
MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
| Applicant | Sanarus Medical, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Sep 23, 2002 |
| Received | Aug 30, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022879
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 12, 2003 | Sanarus Medical Inc Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 (single Device); CD-1000 (5 pack) Terminated |
KNW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.