510(k) K123194 ยท DXC Clamp, Vascular
JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088
| Applicant | North American Rescue Products, Inc., Greer SC, US |
| Decision | Substantially Equivalent, Jan 3, 2013 |
| Received | Oct 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123194
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 26, 2025 | North American Rescue LLC. JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits:
KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550;
KIT, TCCC MODULE ONE - SKILLS, REF: 85-0519;
KIT, MULTI M Open, Classified |
DXC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.