510(k) K881303 ยท DPT Probe, Blood-Flow, Extravascular
TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER
| Applicant | Triton Technology, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 29, 1988 |
| Received | Mar 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881303
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.