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QUICK STAIN WRIGHT'S GIEMSA W/BUFF

K833677 Class I Traditional
Decision Date
1983-11-25
Sponsor / Applicant
J.S. Medical Assoc.

Technical Specification

510(k) Submission ID K833677
Product Code HYF
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.1850
Decision Date 1983-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICK STAIN WRIGHT'S GIEMSA W/BUFF received FDA 510(k) clearance under submission number K833677, sponsored by J.S. Medical Assoc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1983-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code HYF and 21 CFR 864.1850, within the Hematology review panel as a Class I device.