510(k) K072882 ยท LLN Device, Vibration Threshold Measurement
PAIN VISION, MODEL PS-2100
| Applicant | Osachi Co., Ltd., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jan 8, 2009 |
| Received | Oct 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072882
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.