Clearance Summary
FOUR CHANNEL PH PROBE received FDA 510(k) clearance under submission number K853280, sponsored by Akron City Hospital. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1985-12-02.
- Submission: K853280
- Applicant / Sponsor: Akron City Hospital
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.1400
- Decision date: 1985-12-02
Classification & Regulation
This clearance is catalogued under FDA product code FFT and 21 CFR 876.1400, within the Gastroenterology, Urology review panel as a Class I device.