510(k) K922695 ยท LXM Manipulator, Plunger-Like Joint
KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5
| Applicant | Kinetic Technology, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Sep 30, 1992 |
| Received | Jun 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922695
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 5, 2004 | Ameriwater Inc AmeriWater Portable RO+, model numbers MR01 and MR02. The device is a reverse osmosis system for dialysis. Terminated |
FIP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.