510(k) K911202 ยท BSP Needle, Conduction, Anesthetic (W/Wo Introducer)
ATRAUMATIC STANDARD SPROTTE NEEDLE
| Applicant | Pajunk GmbH, Washington DC, US |
| Decision | Substantially Equivalent, May 4, 1992 |
| Received | Mar 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911202
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 13, 2026 | ARROW INTERNATIONAL, LLC Description/REF:
SPINAL ANESTHESIA KIT/ASA-24090-SB;
SPINAL ANESTHESIA KIT/ASA-24103-SB;
SPINAL ANESTHESIA KIT/ASA-25090-SB;
SPINAL ANESTHESIA KIT: 24 GA X 9 CM/ASK-24090-SA;
SPINAL ANESTHESIA KIT: 25 Open, Classified |
BSP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.