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STERILE PROTECTIVE SLEEVE W/TOUGH-BORST

K822290 Class II Traditional
Decision Date
1982-08-31
Sponsor / Applicant
Universal Medical Instrument Corp.

Technical Specification

510(k) Submission ID K822290
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1982-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE PROTECTIVE SLEEVE W/TOUGH-BORST received FDA 510(k) clearance under submission number K822290, sponsored by Universal Medical Instrument 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 1982-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.