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FECAL STAINING KIT

K810875 Class I Traditional
Decision Date
1981-05-01
Sponsor / Applicant
Jayco Pharmaceuticals

Technical Specification

510(k) Submission ID K810875
Product Code KKJ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.1850
Decision Date 1981-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FECAL STAINING KIT received FDA 510(k) clearance under submission number K810875, sponsored by Jayco Pharmaceuticals. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1981-05-01.

Classification & Regulation

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