Clearance Summary
GEL-SCAN DIAGNOSTIC ULTRASOUND COUPLING received FDA 510(k) clearance under submission number K834088, sponsored by Whs Products, 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 1983-12-15.
- Submission: K834088
- Applicant / Sponsor: Whs Products, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.2225
- Decision date: 1983-12-15
Classification & Regulation
This clearance is catalogued under FDA product code HEM and 21 CFR 884.2225, within the Obstetrics/Gynecology review panel as a Class II device.