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FDA 510(k)

CPIVISION DIGITAL IMAGING SYSTEM

K-Number: K061173 · 2006-06-09

ApplicantCommunications & Power Industries Canada, Inc.
Decision Date2006-06-09
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CPIVISION DIGITAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Communications & Power Industries Canada, Inc.. It received FDA 510(k) clearance on 2006-06-09 under 510(k) number K061173. 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 CPIVISION DIGITAL IMAGING SYSTEM?

CPIVISION DIGITAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-06-09. The listed applicant is Communications & Power Industries Canada, Inc.. The 510(k) number is K061173.

When did CPIVISION DIGITAL IMAGING SYSTEM receive FDA 510(k) clearance?

CPIVISION DIGITAL IMAGING SYSTEM received FDA 510(k) clearance on 2006-06-09, under 510(k) number K061173.

Who is the listed applicant for CPIVISION DIGITAL IMAGING SYSTEM?

The FDA 510(k) record lists Communications & Power Industries Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPIVISION DIGITAL IMAGING SYSTEM?

The FDA product code for CPIVISION DIGITAL IMAGING SYSTEM is OWB.

Related Clinical Trials

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Other records listing Communications & Power Industries Canada, 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.

K122726CPI RAD VISIONK083224CPI RAD VISION, MODEL VZW2944XX-YY

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

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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