510(k) K864830 ยท BXN Stimulator, Nerve, Battery-Powered
TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCK
| Applicant | Professional Instruments Co., Houston TX, US |
| Decision | Substantially Equivalent, Jan 12, 1987 |
| Received | Dec 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864830
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.