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FORMALIN BUFFERED

K842982 Class I Traditional
Decision Date
1984-10-01
Sponsor / Applicant
Reagent Laboratory, Inc.

Technical Specification

510(k) Submission ID K842982
Product Code IFP
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1984-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FORMALIN BUFFERED received FDA 510(k) clearance under submission number K842982, sponsored by Reagent Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1984-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code IFP and 21 CFR 864.4010, within the Pathology review panel as a Class I device.