510(k) K893827 ยท FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable
PEAK FLOW RATE METER
| Applicant | Laytech Medical Co., Arlington Heights IL, US |
| Decision | Substantially Equivalent, Aug 11, 1989 |
| Received | May 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893827
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.