510(k) K860126 ยท BXN Stimulator, Nerve, Battery-Powered
STIMUPLEX, NERVE STIMULATOR
| Applicant | Burron Medical Products, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Feb 28, 1986 |
| Received | Jan 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860126
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 11, 2024 | B Braun Medical Inc Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251. Open, Classified |
BXN | None listed |
| Jun 11, 2024 | B Braun Medical Inc Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260 Open, Classified |
BXN | None listed |
| Jun 11, 2024 | B Braun Medical Inc Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278 Open, Classified |
BXN | None listed |
| Jun 11, 2024 | B Braun Medical Inc Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502 Open, Classified |
BXN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.