K122627 is an FDA 510(k) clearance for the GIO DIGITAL PRESSURE GUAGES. This device is classified as a Monitor, Airway Pressure (includes Gauge And/or Alarm) (Class II - Special Controls, product code CAP).
Submitted by Galemed Corp. (Temecula, US). The FDA issued a Cleared decision on August 22, 2013, 359 days after receiving the submission on August 28, 2012.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.2600.
| 510(k) Number | K122627 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 28, 2012 |
| Decision Date | August 22, 2013 |
| Days to Decision | 359 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | CAP — Monitor, Airway Pressure (includes Gauge And/or Alarm) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.2600 |