K900754 is an FDA 510(k) clearance for the RESPIREX 2. This device is classified as a Spirometer, Therapeutic (incentive) (Class II - Special Controls, product code BWF).
Submitted by Diemolding Corp. (Canastota, US). The FDA issued a Cleared decision on March 15, 1990, 27 days after receiving the submission on February 16, 1990.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5690.
| 510(k) Number | K900754 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 16, 1990 |
| Decision Date | March 15, 1990 |
| Days to Decision | 27 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | BWF — Spirometer, Therapeutic (incentive) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5690 |