Clearance Summary
ULTRACELL INSTRUMENT WIPE received FDA 510(k) clearance under submission number K920353, sponsored by Ultracell Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1992-09-15.
- Submission: K920353
- Applicant / Sponsor: Ultracell Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2660
- Decision date: 1992-09-15
Classification & Regulation
This clearance is catalogued under FDA product code HEP and 21 CFR 884.2660, within the Obstetrics/Gynecology review panel as a Class II device.