Clearance Summary
TISCHLER BIOPSY FORCEPS received FDA 510(k) clearance under submission number K926538, 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 1994-02-24.
- Submission: K926538
- Applicant / Sponsor: Thomasville Medical Assoc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4530
- Decision date: 1994-02-24
Classification & Regulation
This clearance is catalogued under FDA product code HFB and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class I device.