510(k) K930689 ยท KHO Fluorometer, For Clinical Use
AUTOBEAD THYROID UPTAKE
| Applicant | Bio-Chem Laboratory Systems, Inc., Lakewood NJ, US |
| Decision | Substantially Equivalent, Nov 10, 1993 |
| Received | Feb 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930689
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.