Id. Store (Release 2.0)

FDA 510(k) K973413 · I.S.G. Technologies, Inc.

Substantially Equivalent

510(k) numberK973413

Submission

Device name
Id. Store (Release 2.0)
Applicant
I.S.G. Technologies, Inc.
Mississauga Ontario, CA
Received
September 9, 1997
Decision date
November 25, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LMB – Device, Digital Image Storage, Radiological
Device class
Class I (low risk)
Regulation
21 CFR 892.2010
Specialty
Radiology

Medical image storage hardware is a device that provides electronic maintenance and access functions for medical images.

Other 510(k)s with product code LMB

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K983447Wise (II) Image Management SystemLMB · Special Sectra-Imtec AB10/29/1998SE
K980243Parameter Developments Dicom Archival Server, (Das)/Dicom Intranet Service (Dis)LMB · Traditional Parameter Developments, Inc.04/03/1998SE
K973463Olicon Imaging Systems, Inc. Archive Systems, NT Archive, 02ARCHIVE, ArchiveLMB · Traditional O Tech, Inc.12/02/1997SE
K972380Kodak Digital Science (KDS) Medical Image and Information Library (Miil)LMB · Traditional Eastman Kodak Company09/11/1997SE
K971848TDK Medical Grade Cd-RLMB · Traditional Tdk Electronics Corporation of America08/15/1997SE
K971451Wise Image Management SystemLMB · Traditional O Tech, Inc.06/26/1997SE
K963936Accesspoint, Med E-Mail, Dicom ReaderLMB · Traditional Biosound, Inc.03/31/1997SE
K964803Univision Echocardiology SystemLMB · Traditional Network Concepts, Inc.02/11/1997SE

More from Network Concepts, Inc.

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K980684VR NetserveLMD · Traditional 05/06/1998SE
K970865Isg Family of Viewing WandsHAW · Traditional 06/04/1997SE
K960714Isg Viewing WandHAW · Traditional 05/29/1996SE
K941933Isg Medical Imaging Family of Workstations (Mifw)LLZ · Traditional 07/29/1994SE
K911783Allegro Viewing WandLLZ · Traditional 04/07/1994SE
K901679Resubmitted Isg 3DMV WorkstationLLZ · Traditional 05/29/1990SE
K872150I.S.G. 3DMV WorkstationJAK · Traditional 08/12/1987SE

Questions and answers

When was Id. Store (Release 2.0) cleared by the FDA?

Id. Store (Release 2.0) (K973413) received a 510(k) decision of Substantially Equivalent on November 25, 1997, 77 days after the submission was received.

What is the product code of K973413?

The FDA product code is LMB – Device, Digital Image Storage, Radiological, a Class I (low risk) device regulated under 21 CFR 892.2010.