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OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE

K973463 Class I Traditional
Decision Date
1997-12-02
Sponsor / Applicant
O Tech, Inc.

Technical Specification

510(k) Submission ID K973463
Product Code LMB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2010
Decision Date 1997-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE received FDA 510(k) clearance under submission number K973463, sponsored by O Tech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code LMB and 21 CFR 892.2010, within the Radiology review panel as a Class I device.