K100687 is an FDA 510(k) clearance for the VITALOGRAPH HAND HELD SPIROMETER, MODEL 2120. This device is classified as a Spirometer, Diagnostic (Class II - Special Controls, product code BZG).
Submitted by Vitalograph (Ireland) , Ltd. (Ennis, Co. Clare, IE). The FDA issued a Cleared decision on October 16, 2010, 220 days after receiving the submission on March 10, 2010.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1840.
| 510(k) Number | K100687 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 10, 2010 |
| Decision Date | October 16, 2010 |
| Days to Decision | 220 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BZG — Spirometer, Diagnostic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1840 |