510(k) K953077 ยท CDF Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM
| Applicant | Beckman Instruments, Inc., Brea CA, US |
| Decision | Substantially Equivalent, Jan 5, 1996 |
| Received | Jun 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953077
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.