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SERIES 810 PLATELET ANALYZER

K803128 Class II Traditional
Decision Date
1981-04-03
Sponsor / Applicant
J.T. Baker Chemical Co.

Technical Specification

510(k) Submission ID K803128
Product Code GKL
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5200
Decision Date 1981-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERIES 810 PLATELET ANALYZER received FDA 510(k) clearance under submission number K803128, sponsored by J.T. Baker Chemical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1981-04-03.

Classification & Regulation

This clearance is catalogued under FDA product code GKL and 21 CFR 864.5200, within the Hematology review panel as a Class II device.