510(k) K222525 ยท BZG Spirometer, Diagnostic
Alveoair Digital Spirometer
| Applicant | Roundworks Technologies Private Limited, Wakad, Pune, IN |
| Decision | Substantially Equivalent, Aug 28, 2023 |
| Received | Aug 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222525
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.