510(k) K990522 ยท OLV Standard Polysomnograph With Electroencephalograph
WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WITHOUT, PULSE OXIMETRY,CARDINAL DIGITAL EEG AND SLEEP ACQUIS
| Applicant | Lamont Medical, Inc., Madison WI, US |
| Decision | Substantially Equivalent, May 19, 1999 |
| Received | Feb 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990522
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.