510(k) K911221 ยท BSP Needle, Conduction, Anesthetic (W/Wo Introducer)
ATRAUMATIC SPECIAL SPROTTE NEEDLE
| Applicant | Pajunk GmbH, Washington DC, US |
| Decision | Substantially Equivalent, Jul 24, 1992 |
| Received | Mar 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911221
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.