510(k) K863607 ยท LLN Device, Vibration Threshold Measurement
VIBRATRON II, VIBRATION SENSITIVITY TESTER
| Applicant | Sensortek, Inc., Clifton NJ, US |
| Decision | Substantially Equivalent, Dec 3, 1986 |
| Received | Sep 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863607
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.