meddevicedb.com FDA Device Reference

SLIDE, LAB-TEK COVERED MICRO

K760278 Class I Traditional
Decision Date
1976-08-30
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K760278
Product Code KEW
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3010
Decision Date 1976-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLIDE, LAB-TEK COVERED MICRO received FDA 510(k) clearance under submission number K760278, 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 1976-08-30.

Classification & Regulation

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