510(k) K910624 ยท LLN Device, Vibration Threshold Measurement
CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4
| Applicant | Wr Medical Electronics Co., Stillwater MN, US |
| Decision | Substantially Equivalent, Jan 17, 1992 |
| Received | Feb 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910624
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.