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FDA 510(k)

PVMED DDR 2520 DIGITAL IMAGING SYSTEM

K-Number: K072766 · 2007-12-11

ApplicantPortavision Medical
Decision Date2007-12-11
Product CodeIXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PVMED DDR 2520 DIGITAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Portavision Medical. It received FDA 510(k) clearance on 2007-12-11 under 510(k) number K072766. The device is classified under product code IXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVMED DDR 2520 DIGITAL IMAGING SYSTEM?

PVMED DDR 2520 DIGITAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-12-11. The listed applicant is Portavision Medical. The 510(k) number is K072766.

When did PVMED DDR 2520 DIGITAL IMAGING SYSTEM receive FDA 510(k) clearance?

PVMED DDR 2520 DIGITAL IMAGING SYSTEM received FDA 510(k) clearance on 2007-12-11, under 510(k) number K072766.

Who is the listed applicant for PVMED DDR 2520 DIGITAL IMAGING SYSTEM?

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

What is the FDA product code for PVMED DDR 2520 DIGITAL IMAGING SYSTEM?

The FDA product code for PVMED DDR 2520 DIGITAL IMAGING SYSTEM is IXK.

Related Clinical Trials

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Related Devices (Code: IXK)

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.

K093640DIGITAL X-RAY DETECTORS FAMILY KRC AND DIRAElectron Jsco.K042779RADIOTHERAPY SOLUTION BASED ON CRAgfa Corp.K032654PORT CASSETTEOrex Computed Radiography, Ltd.K003689CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31Canon USA, Inc.K000159AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLOAgfa Corp.K942561FUJI FCR IMAGE PROCESSING UNIT IP-U515Fujifilm Medical System U.S.A., 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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