Clearance Summary
ULCUFLEX HYDROCOLOID POWDER received FDA 510(k) clearance under submission number K920366, sponsored by Industrias Palex C/O Dma Med-Chem 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 1992-03-26.
- Submission: K920366
- Applicant / Sponsor: Industrias Palex C/O Dma Med-Chem Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5090
- Decision date: 1992-03-26
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.