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FDA 510(k)

LR DICOM CONTROLLER

K-Number: K022658 · 2002-09-06

ApplicantAgfa Corp.
Decision Date2002-09-06
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LR DICOM CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Agfa Corp.. It received FDA 510(k) clearance on 2002-09-06 under 510(k) number K022658. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LR DICOM CONTROLLER?

LR DICOM CONTROLLER is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is Agfa Corp.. The 510(k) number is K022658.

When did LR DICOM CONTROLLER receive FDA 510(k) clearance?

LR DICOM CONTROLLER received FDA 510(k) clearance on 2002-09-06, under 510(k) number K022658.

Who is the listed applicant for LR DICOM CONTROLLER?

The FDA 510(k) record lists Agfa Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LR DICOM CONTROLLER?

The FDA product code for LR DICOM CONTROLLER is LMC.

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Other records listing Agfa Corp. 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.

K063421DX-SIK053458WEB1000K050751IMPAX ORTHOPAEDIC WORKSTATION, MODEL IMPAX ES 5.XK050810AGFA CR50.0K042779RADIOTHERAPY SOLUTION BASED ON CRK041701AFGA CR25.0 COMPUTED RADIOGRAPHY SYSTEM

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Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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