Clearance Summary
DERMA HOOD received FDA 510(k) clearance under submission number K131338, sponsored by Globalmedia Group, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2013-07-10.
- Submission: K131338
- Applicant / Sponsor: Globalmedia Group, LLC
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6320
- Decision date: 2013-07-10
Classification & Regulation
This clearance is catalogued under FDA product code PEQ and 21 CFR 880.6320, within the General Hospital review panel as a Class I device.