K895953 is an FDA 510(k) clearance for the WRIGHT VENTILOMETER VM-1. This device is classified as a Spirometer, Diagnostic (Class II - Special Controls, product code BZG).
Submitted by Clement Clarke, Inc. (England, GB). The FDA issued a Cleared decision on February 2, 1990, 114 days after receiving the submission on October 11, 1989.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1840.
| 510(k) Number | K895953 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 11, 1989 |
| Decision Date | February 02, 1990 |
| Days to Decision | 114 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | BZG — Spirometer, Diagnostic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1840 |