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CHANG MEDIUM

K812820 Class I Traditional
Decision Date
1981-11-10
Sponsor / Applicant
Hana Biologics, Inc.

Technical Specification

510(k) Submission ID K812820
Product Code KIT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.2220
Decision Date 1981-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHANG MEDIUM received FDA 510(k) clearance under submission number K812820, sponsored by Hana Biologics, 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 1981-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code KIT and 21 CFR 864.2220, within the Hematology review panel as a Class I device.