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FDA 510(k)

CPI RAD VISION

K-Number: K122726 · 2013-02-15

ApplicantCommunications & Power Industries Canada, Inc.
Decision Date2013-02-15
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CPI RAD VISION 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 2013-02-15 under 510(k) number K122726. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPI RAD VISION?

CPI RAD VISION is a medical device that received FDA 510(k) clearance on 2013-02-15. The listed applicant is Communications & Power Industries Canada, Inc.. The 510(k) number is K122726.

When did CPI RAD VISION receive FDA 510(k) clearance?

CPI RAD VISION received FDA 510(k) clearance on 2013-02-15, under 510(k) number K122726.

Who is the listed applicant for CPI RAD VISION?

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 CPI RAD VISION?

The FDA product code for CPI RAD VISION is KPR.

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 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.

K083224CPI RAD VISION, MODEL VZW2944XX-YYK061173CPIVISION DIGITAL IMAGING SYSTEM

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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