510(k) K885327 ยท LMB Device, Digital Image Storage, Radiological
PHILIPS DIGITAL CARDIAC IMAGING (DCI) SYSTEM
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, May 11, 1989 |
| Received | Dec 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885327
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.