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REPROCESSED COMPRESSION SLEEVES

K053316 Class II Traditional
Decision Date
2006-02-13
Sponsor / Applicant
Alliance Medical Corp.

Technical Specification

510(k) Submission ID K053316
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 2006-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED COMPRESSION SLEEVES received FDA 510(k) clearance under submission number K053316, sponsored by Alliance Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code JOW and 21 CFR 870.5800, within the Cardiovascular review panel as a Class II device.