510(k) K932645 ยท LNH System, Nuclear Magnetic Resonance Imaging
PHILIPS GYROSCAN TN 15
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Dec 13, 1993 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932645
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 12, 2003 | Philips Medical Systems Gyroscan ACS-NT system Terminated |
LNH | None listed |
| Sep 12, 2003 | Philips Medical Systems Gyroscan ACS-NT with software versions R6x, R7x, R8x Terminated |
LNH | None listed |
| Sep 12, 2003 | Philips Medical Systems Gyroscan NT-Intera Terminated |
LNH | None listed |
| Sep 12, 2003 | Philips Medical Systems Gyroscan Intera 1.0T & 1.5T Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.