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MICROSCOPE SLIDES PRECOATED

K890042 Class I Traditional
Decision Date
1989-01-13
Sponsor / Applicant
Stat Path

Technical Specification

510(k) Submission ID K890042
Product Code KEW
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3010
Decision Date 1989-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROSCOPE SLIDES PRECOATED received FDA 510(k) clearance under submission number K890042, sponsored by Stat Path. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1989-01-13.

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.