510(k) K933200 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
OLYMPUS PBD STENTS
| Applicant | Olympus Corp., Lake Success NY, US |
| Decision | Substantially Equivalent, Apr 5, 1995 |
| Received | Jul 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933200
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 4, 2021 | Aomori Olympus Co., Ltd. PBD-203-0703 BILIARY STENT, model no. PBD-203-0703 - Product Usage: Used with endoscopes for endoscopic retrograde biliary drainage. Terminated |
FGE | None listed |
| Jan 4, 2021 | Aomori Olympus Co., Ltd. PBD-203-0704 BILIARY STENT, model no. PBD-203-0704 -Product Usage: Used with endoscopes for endoscopic retrograde biliary drainage. Terminated |
FGE | None listed |
| Jan 4, 2021 | Aomori Olympus Co., Ltd. PBD-203-0707 BILIARY STENT, model no. PBD-203-0707 -Product Usage: Used with endoscopes for endoscopic retrograde biliary drainage. Terminated |
FGE | None listed |
| Jan 4, 2021 | Aomori Olympus Co., Ltd. PBD-203-0710 BILIARY STENT, model no. PBD-203-0710 -Product Usage: Used with endoscopes for endoscopic retrograde biliary drainage. Terminated |
FGE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.