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MICROSCOPE STAGE HEATER

K881467 Class I Traditional
Decision Date
1988-04-18
Sponsor / Applicant
Cryodyne Technologies, Inc.

Technical Specification

510(k) Submission ID K881467
Product Code KEJ
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3600
Decision Date 1988-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROSCOPE STAGE HEATER received FDA 510(k) clearance under submission number K881467, sponsored by Cryodyne Technologies, 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 1988-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code KEJ and 21 CFR 864.3600, within the Pathology review panel as a Class I device.