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FDA 510(k)

VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM

K-Number: K915094 · 1991-12-27

ApplicantVortech Data, Inc.
Decision Date1991-12-27
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vortech Data, Inc.. It received FDA 510(k) clearance on 1991-12-27 under 510(k) number K915094. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM?

VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is Vortech Data, Inc.. The 510(k) number is K915094.

When did VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM receive FDA 510(k) clearance?

VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM received FDA 510(k) clearance on 1991-12-27, under 510(k) number K915094.

Who is the listed applicant for VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM?

The FDA 510(k) record lists Vortech Data, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM?

The FDA product code for VORTECH'S IMAGE ARCHIVAL AND RETRIEVAL SYSTEM is LMB.

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Other records listing Vortech Data, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K924366PERSONAL DISPLAY SYSTEMK925097VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)K924229VG-A MIGK922310VORTECH'S PERSONAL DISPLAY SYSTEMK915362VORTECH'S FILM DIGITIZER, FD-1K914834VORTECH 3M NETWORK PRINTING

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Related Devices (Code: LMB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K992131SAMSUNG RAYPAX LONG TERM ARCHIVESamsung Sds Co., Ltd.K984405ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000Intracom Corp.K983447WISE (II) IMAGE MANAGEMENT SYSTEMSectra-Imtec ABK980243PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)Parameter Developments, Inc.K973463OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVEO Tech, Inc.K973413ID. STORE (RELEASE 2.0)I.S.G. Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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