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LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)

K883599 Class I Traditional
Decision Date
1988-09-02
Sponsor / Applicant
Innovative Medical Systems, Inc.

Technical Specification

510(k) Submission ID K883599
Product Code IEO
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3875
Decision Date 1988-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) received FDA 510(k) clearance under submission number K883599, sponsored by Innovative Medical Systems, 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 1988-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code IEO and 21 CFR 864.3875, within the Pathology review panel as a Class I device.