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HEMOHLOBIN A2 CONTROL-LYOPHILIZED

K801410 Class II Traditional
Decision Date
1980-07-21
Sponsor / Applicant
Isolab, Inc.

Technical Specification

510(k) Submission ID K801410
Product Code JPD
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7400
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOHLOBIN A2 CONTROL-LYOPHILIZED received FDA 510(k) clearance under submission number K801410, 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 1980-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code JPD and 21 CFR 864.7400, within the Hematology review panel as a Class II device.