Clearance Summary
VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT received FDA 510(k) clearance under submission number K926429, sponsored by Thomasville Medical Assoc.. 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 1994-02-28.
- Submission: K926429
- Applicant / Sponsor: Thomasville Medical Assoc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4520
- Decision date: 1994-02-28
Classification & Regulation
This clearance is catalogued under FDA product code HDF and 21 CFR 884.4520, within the Obstetrics/Gynecology review panel as a Class I device.