AS-10, CXDI-401RF
K-Number: K171194 · 2017-05-24
ApplicantCanon, Inc.
Decision Date2017-05-24
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
AS-10, CXDI-401RF is a medical device manufactured by Canon, Inc.. It received FDA 510(k) clearance on 2017-05-24 under approval number K171194. 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 AS-10, CXDI-401RF?
AS-10, CXDI-401RF is a medical device that received FDA 510(k) clearance on 2017-05-24. It is manufactured by Canon, Inc.. The 510(k) number is K171194.
When was AS-10, CXDI-401RF approved by the FDA?
AS-10, CXDI-401RF received FDA 510(k) clearance on 2017-05-24, under approval number K171194.
What company makes AS-10, CXDI-401RF?
AS-10, CXDI-401RF is manufactured by Canon, Inc..
What is the FDA product code for AS-10, CXDI-401RF?
The FDA product code for AS-10, CXDI-401RF is OWB.
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K190368Enhanced Feature Software Pack CXDI Series
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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.