meddevicedb.com FDA Device Reference

PLATELET CONTROLS NORMAL & ABNORMAL

K771588 Class II Traditional
Decision Date
1977-08-25
Sponsor / Applicant
Dade, Baxter Travenol Diagnostics, Inc.

Technical Specification

510(k) Submission ID K771588
Product Code GJP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 1977-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLATELET CONTROLS NORMAL & ABNORMAL received FDA 510(k) clearance under submission number K771588, sponsored by Dade, Baxter Travenol Diagnostics, 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 1977-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code GJP and 21 CFR 864.8625, within the Hematology review panel as a Class II device.