Clearance Summary
ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T) received FDA 510(k) clearance under submission number K970799, sponsored by Alexander Mfg. Co.. 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 1997-05-14.
- Submission: K970799
- Applicant / Sponsor: Alexander Mfg. Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1997-05-14
Classification & Regulation
This clearance is catalogued under FDA product code LIF and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.