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FDA 510(k)

ANGIOTEC IMAGE MANAGEMENT SYSTEM

K-Number: K903806 · 1990-11-23

ApplicantAndros Analyzers, Inc.
Decision Date1990-11-23
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIOTEC IMAGE MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Andros Analyzers, Inc.. It received FDA 510(k) clearance on 1990-11-23 under 510(k) number K903806. 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 ANGIOTEC IMAGE MANAGEMENT SYSTEM?

ANGIOTEC IMAGE MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-23. The listed applicant is Andros Analyzers, Inc.. The 510(k) number is K903806.

When did ANGIOTEC IMAGE MANAGEMENT SYSTEM receive FDA 510(k) clearance?

ANGIOTEC IMAGE MANAGEMENT SYSTEM received FDA 510(k) clearance on 1990-11-23, under 510(k) number K903806.

Who is the listed applicant for ANGIOTEC IMAGE MANAGEMENT SYSTEM?

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

What is the FDA product code for ANGIOTEC IMAGE MANAGEMENT SYSTEM?

The FDA product code for ANGIOTEC IMAGE MANAGEMENT SYSTEM is LMB.

Related Clinical Trials

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Other records listing Andros Analyzers, 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.

K893476ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.K892869ANGIOTEC ZX DIGITAL IMAGE PROCESSORK891485ANGIOTEC FMX-2220 SYSTEMK852463ANDROS ANALYZERS AIRWAY ADAPTER

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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