meddevicedb.com FDA Device Reference

ZINC FORMALIN CONCENTRATE

K882268 Class I Traditional
Decision Date
1988-06-15
Sponsor / Applicant
Anatech, Ltd.

Technical Specification

510(k) Submission ID K882268
Product Code IGG
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1988-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZINC FORMALIN CONCENTRATE received FDA 510(k) clearance under submission number K882268, sponsored by Anatech, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1988-06-15.

Classification & Regulation

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