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VERIFY FLASH INTEGRATOR

K051101 Class II Traditional
Decision Date
2005-12-06
Sponsor / Applicant
Albert Browne , Ltd.

Technical Specification

510(k) Submission ID K051101
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2005-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY FLASH INTEGRATOR received FDA 510(k) clearance under submission number K051101, sponsored by Albert Browne , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.