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FDA 510(k)

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl

K-Number: K232298 · 2024-04-26

ApplicantCanon, Inc.
Decision Date2024-04-26
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is a medical device manufactured by Canon, Inc.. It received FDA 510(k) clearance on 2024-04-26 under approval number K232298. 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 DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is a medical device that received FDA 510(k) clearance on 2024-04-26. It is manufactured by Canon, Inc.. The 510(k) number is K232298.

When was DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl approved by the FDA?

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl received FDA 510(k) clearance on 2024-04-26, under approval number K232298.

What company makes DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is manufactured by Canon, Inc..

What is the FDA product code for DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

The FDA product code for DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is OWB.

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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.

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