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FDA 510(k)

CANON, MODEL URS-50RF

K-Number: K093688 · 2010-02-04

ApplicantVirtual Imaging, Inc.
Decision Date2010-02-04
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CANON, MODEL URS-50RF is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Imaging, Inc.. It received FDA 510(k) clearance on 2010-02-04 under 510(k) number K093688. 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 CANON, MODEL URS-50RF?

CANON, MODEL URS-50RF is a medical device that received FDA 510(k) clearance on 2010-02-04. The listed applicant is Virtual Imaging, Inc.. The 510(k) number is K093688.

When did CANON, MODEL URS-50RF receive FDA 510(k) clearance?

CANON, MODEL URS-50RF received FDA 510(k) clearance on 2010-02-04, under 510(k) number K093688.

Who is the listed applicant for CANON, MODEL URS-50RF?

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

What is the FDA product code for CANON, MODEL URS-50RF?

The FDA product code for CANON, MODEL URS-50RF is OWB.

Related Clinical Trials

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Other records listing Virtual Imaging, 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.

K092439CANON DIGITAL FLUOROSCOPY AND RADIOGRAPHY, MODEL CXDI-50RFK092280CYPHER DICOM PRINT SOLUTIONK083725RADPRO IONK070390FLUOROPRO RF DIGITAL IMAGING SYSTEM

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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