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SICKLING HEMOGLOBIN CONTROLS, NORMAL

K842152 Class II Traditional
Decision Date
1984-09-09
Sponsor / Applicant
Isolab, Inc.

Technical Specification

510(k) Submission ID K842152
Product Code GHM
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7825
Decision Date 1984-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SICKLING HEMOGLOBIN CONTROLS, NORMAL received FDA 510(k) clearance under submission number K842152, sponsored by Isolab, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1984-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code GHM and 21 CFR 864.7825, within the Hematology review panel as a Class II device.