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VERIFY 3-10 MIN FLASH INTEGRATOR

K060066 Class II Traditional
Decision Date
2006-03-24
Sponsor / Applicant
Albert Browne , Ltd.

Technical Specification

510(k) Submission ID K060066
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2006-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY 3-10 MIN FLASH INTEGRATOR received FDA 510(k) clearance under submission number K060066, 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 2006-03-24.

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.