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FDA 510(k)

CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D

K-Number: K871119 · 1987-03-31

ApplicantCanon USA, Inc.
Decision Date1987-03-31
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K871119. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D?

CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Canon USA, Inc.. The 510(k) number is K871119.

When did CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D receive FDA 510(k) clearance?

CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D received FDA 510(k) clearance on 1987-03-31, under 510(k) number K871119.

Who is the listed applicant for CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D?

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

What is the FDA product code for CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D?

The FDA product code for CANON X-RAY IMAGE DISTRIBUTOR CXI-3-3D is JAA.

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Other records listing Canon USA, 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.

K090623DIGITAL RADIOGRAPHY CXDI-40G COMPACTK033624PACS SOFTWARE SOLUTION 2003K031633CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40CK031629CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGIK023750CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40GK023586DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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