510(k) K911419 ยท LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
SENSITITRE ARIS MODULE
| Applicant | Sensititre , Ltd., Westlake OH, US |
| Decision | Substantially Equivalent, Jul 1, 1992 |
| Received | Apr 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911419
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.