510(k) K894127 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
LUMISCOPE MODEL 1000/APCC MODEL 1000
| Applicant | Lumiscope Co., Inc., Edison NJ, US |
| Decision | Substantially Equivalent, Sep 6, 1989 |
| Received | Jun 12, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894127
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.