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HEMATIC BLOOD MIXER

K802608 Class I Traditional
Decision Date
1980-12-11
Sponsor / Applicant
Helmer Labs, Inc.

Technical Specification

510(k) Submission ID K802608
Product Code KSQ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9195
Decision Date 1980-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMATIC BLOOD MIXER received FDA 510(k) clearance under submission number K802608, sponsored by Helmer Labs, 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 1980-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code KSQ and 21 CFR 864.9195, within the Hematology review panel as a Class I device.