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TISSUE PROCESSING CASSETTES & ACCESS

K813430 Class I Traditional
Decision Date
1981-12-29
Sponsor / Applicant
American Optical Corp.

Technical Specification

510(k) Submission ID K813430
Product Code IDL
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3010
Decision Date 1981-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE PROCESSING CASSETTES & ACCESS received FDA 510(k) clearance under submission number K813430, sponsored by American Optical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1981-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code IDL and 21 CFR 864.3010, within the Pathology review panel as a Class I device.