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LX120 TISSUE PROCESSOR

K851054 Class I Traditional
Decision Date
1985-05-15
Sponsor / Applicant
Innovative Medical Systems, Inc.

Technical Specification

510(k) Submission ID K851054
Product Code IEO
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.3875
Decision Date 1985-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LX120 TISSUE PROCESSOR received FDA 510(k) clearance under submission number K851054, 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 1985-05-15.

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.