Clearance Summary
DYNASORB received FDA 510(k) clearance under submission number K951561, sponsored by Dermarx Corp.. 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 1995-09-01.
- Submission: K951561
- Applicant / Sponsor: Dermarx Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5090
- Decision date: 1995-09-01
Classification & Regulation
This clearance is catalogued under FDA product code KMF and 21 CFR 880.5090, within the General Hospital review panel as a Class I device.