510(k) K896121 ยท BZG Spirometer, Diagnostic
SCHILLER MODEL SP-200 SPIROVIT(TM)
| Applicant | Schiller America, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jan 9, 1990 |
| Received | Oct 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896121
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.