510(k) K982960 ยท KNW Instrument, Biopsy
MEICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSABLE AUTOMATIC BIOPSY INSTRUMENT
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Sep 23, 1998 |
| Received | Aug 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982960
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 20, 2024 | Argon Medical Devices, Inc BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-2080-02, 360-2080-03, 370-1080-01, 370-1080-02, 370 Open, Classified |
KNW | None listed |
| Oct 8, 2010 | Medical Device Technologies, Inc. Tru-Core II Disposable Automatic Biopsy Instrument and Tru-Core II URO Disposable Automatic Biopsy Instrument. The Tru-Core Disposable Automatic Biopsy Instrument is used to obtain multiple core samp Terminated |
MJG | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.