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F.A. MOUNTING MEDIUM

K781388 Class I Traditional
Decision Date
1978-08-21
Sponsor / Applicant
Flow Laboratories, Inc.

Technical Specification

510(k) Submission ID K781388
Product Code KEQ
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1978-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

F.A. MOUNTING MEDIUM received FDA 510(k) clearance under submission number K781388, sponsored by Flow 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 1978-08-21.

Classification & Regulation

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