510(k) K020669 ยท DTB Permanent Pacemaker Electrode
PERMANENT PACING LEAD, MODELS PETITE, PETITE R, J, RJ, PETITE B, RB, JB, RJB
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 28, 2002 |
| Received | Mar 1, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020669
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.