510(k) K933278 ยท KRG Programmer, Pacemaker
INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
| Applicant | Intermedics, Inc., Angleton TX, US |
| Decision | Substantially Equivalent, Mar 15, 1995 |
| Received | Jun 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933278
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.