510(k) K102081 ยท FZP Clip, Implantable
ENDOSCOPIC CLIP SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Aug 6, 2010 |
| Received | Jul 26, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102081
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 22, 2018 | Aesculap Implant Systems LLC DS Titanium Ligation Clip, used in laparoscopic surgery Terminated |
FZP | None listed |
| Jan 22, 2018 | Aesculap Implant Systems LLC DS Titanium Ligation Clip Appliers, used in laparoscopic surgery Terminated |
FZP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.