510(k) K043130 ยท CAZ Anesthesia Conduction Kit
MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS
| Applicant | Pajunk GmbH, Corvallis OR, US |
| Decision | Substantially Equivalent, Dec 21, 2004 |
| Received | Nov 12, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K043130
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.