DERMA HOOD— 510(k) K131338
Substantially EquivalentGlobalmedia Group, LLC
FDA 510(k) clearance K131338 for DERMA HOOD, Substantially Equivalent on 2013-07-10. Applicant: Globalmedia Group, LLC. Device class: 1.
Clearance details
- Applicant
- Globalmedia Group, LLC
- Product code
- Code PEQ
- Device class
- Class 1
- Regulation
- 21 CFR 880.6320
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Scottsdale, AZ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.