510(k) K880452 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE
| Applicant | Lumiscope Co., Inc., Edison NJ, US |
| Decision | Substantially Equivalent, Mar 24, 1988 |
| Received | Feb 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880452
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.