510(k) K980226 ยท KNW Instrument, Biopsy
MANAN PRO-MAG AUTOMATIC BIOPSY SYSTEM
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Feb 18, 1998 |
| Received | Jan 22, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980226
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2010 | Medical Device Technologies, Inc. Angiotech Soft Tissue Biopsy Needle Core:
A) Pro-Mag "Short Throw" Biopsy Needle, and Pro-Mag Biopsy Needle. STERILE.
Product Number: 765114080, 765116120, 765114120, 765118080, 765118120, 765014 Terminated |
KNW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.