510(k) K002040 ยท HRX Arthroscope
FMS SOLO
| Applicant | Future Medical Systems, Inc., Glen Burnie MD, US |
| Decision | Substantially Equivalent, Sep 11, 2000 |
| Received | Jul 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002040
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 8, 2013 | DePuy Mitek, Inc., a Johnson & Johnson Co. DePuy Mitek FMS Outflow Tubing with One-Way valve
Product Code:284649
Product Usage: The Intermediary Tubing for FMS Fluid Management Systems connects the Inflow Tubing to the arthroscopic sheath du Terminated |
HRX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.