Clearance Summary
COLPOSCOPE (DYNATECH COLPOSCOPE-MODEL I received FDA 510(k) clearance under submission number K760763, sponsored by Dynatech Cryomedical Co.. 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 1976-10-20.
- Submission: K760763
- Applicant / Sponsor: Dynatech Cryomedical Co.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1630
- Decision date: 1976-10-20
Classification & Regulation
This clearance is catalogued under FDA product code HEX and 21 CFR 884.1630, within the Obstetrics/Gynecology review panel as a Class II device.