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FDA 510(k)

RFVISION, MODEL 9.9D

K-Number: K080847 · 2008-08-06

ApplicantAlmana Medical Imaging
Decision Date2008-08-06
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RFVISION, MODEL 9.9D is the device name listed in this FDA 510(k) record. The listed applicant is Almana Medical Imaging. It received FDA 510(k) clearance on 2008-08-06 under 510(k) number K080847. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RFVISION, MODEL 9.9D?

RFVISION, MODEL 9.9D is a medical device that received FDA 510(k) clearance on 2008-08-06. The listed applicant is Almana Medical Imaging. The 510(k) number is K080847.

When did RFVISION, MODEL 9.9D receive FDA 510(k) clearance?

RFVISION, MODEL 9.9D received FDA 510(k) clearance on 2008-08-06, under 510(k) number K080847.

Who is the listed applicant for RFVISION, MODEL 9.9D?

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

What is the FDA product code for RFVISION, MODEL 9.9D?

The FDA product code for RFVISION, MODEL 9.9D is OWB.

Related Clinical Trials

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.

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Other records listing Almana Medical Imaging 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.

K100001MOBIVISIONK082064RADVISION ET DIAGNOSTIC X-RAY SYSTEMK080614DR VISION NEO, DR VISION DOUK072659RAD VISION, MODELS E AND EU

Related Devices (Code: OWB)

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.

K253726uAngio AVIVA CXShanghai United Imaging Healthcare Co., Ltd.K261413EXTRON 3;EXTRON 6DRTECH CorporationK254205Zenition 30Philips Medical Systems Nederland B.V.K260607Shield System (Siemens 30x40)Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.

Official Source

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

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