510(k) K832397 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
HYBRITECH 405-500 NM FILTER MODULE
| Applicant | Hybritech, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1983 |
| Received | Jul 20, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832397
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.