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CORTI-SHURE

K791700 Class II Traditional
Decision Date
1979-10-01
Sponsor / Applicant
Nuclear Medical Laboratories, Inc.

Technical Specification

510(k) Submission ID K791700
Product Code CGR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1205
Decision Date 1979-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORTI-SHURE received FDA 510(k) clearance under submission number K791700, sponsored by Nuclear Medical Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1979-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code CGR and 21 CFR 862.1205, within the Clinical Chemistry review panel as a Class II device.