510(k) K943381 ยท IWE Monitor, Patient Position, Light-Beam
LASER ALIGNMENT TOOL
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Aug 9, 1994 |
| Received | Jul 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943381
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.