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ALEXANDER BOX, BATTERY, RECHARGEABLE

K963305 Class II Traditional
Decision Date
1997-04-17
Sponsor / Applicant
Alexander Mfg. Co.

Technical Specification

510(k) Submission ID K963305
Product Code BWA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1997-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALEXANDER BOX, BATTERY, RECHARGEABLE received FDA 510(k) clearance under submission number K963305, 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 1997-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code BWA and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.