510(k) K896359 ยท CCL Analyzer, Gas, Oxygen, Gaseous-Phase
AG-820PA FI02 MODULE
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 9, 1990 |
| Received | Nov 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896359
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.