510(k) K242228 ยท KNW Instrument, Biopsy
Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01)
| Applicant | Triopsy Medical, Inc., Mankato MN, US |
| Decision | Substantially Equivalent, Jan 10, 2025 |
| Received | Jul 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242228
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.