510(k) K932281 ยท GCT Light Source, Endoscope, Xenon Arc
VERRES NEEDLE
| Applicant | Surgeon Surgical Instrumentation, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Aug 6, 1993 |
| Received | May 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932281
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.