GIO DIGITAL PRESSURE GUAGES— 510(k) K122627
Substantially EquivalentGalemed Corp.
FDA 510(k) clearance K122627 for GIO DIGITAL PRESSURE GUAGES, Substantially Equivalent on 2013-08-22. Applicant: Galemed Corp.. Device class: 2.
Clearance details
- Applicant
- Galemed Corp.
- Product code
- Code CAP
- Device class
- Class 2
- Regulation
- 21 CFR 868.2600
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Temecula, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.