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HISTOLOGICAL EMBEDDING MEDIA

K803241 Class I Traditional
Decision Date
1981-01-28
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K803241
Product Code KEO
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1981-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HISTOLOGICAL EMBEDDING MEDIA received FDA 510(k) clearance under submission number K803241, sponsored by Miles Laboratories, 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 1981-01-28.

Classification & Regulation

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