Clearance Summary
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 received FDA 510(k) clearance under submission number K980224, sponsored by Alexander Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1998-04-02.
- Submission: K980224
- Applicant / Sponsor: Alexander Mfg. Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1998-04-02
Classification & Regulation
This clearance is catalogued under FDA product code MOQ and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.