510(k) K972777 ยท MJN Catheter, Intravascular Occluding, Temporary
TEMPORARY OCCLUSION BALLOON SYSTEM
| Applicant | Percu Surge, Inc., Sunnyvale CA, US |
| Decision | Unknown, Mar 11, 1998 |
| Received | Jul 25, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972777
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.