510(k) K022121 ยท OLV Standard Polysomnograph With Electroencephalograph
PSG INPUT BOX, MODEL JE-912AK
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Jul 29, 2002 |
| Received | Jul 1, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022121
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.