510(k) K011988 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
SURGICAL LIGHTSTIC 180, MODEL 180 L, MODEL 180 C
| Applicant | Cardiofocus, Inc., Norton MA, US |
| Decision | Substantially Equivalent, Sep 20, 2001 |
| Received | Jun 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011988
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.