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FDA 510(k)

FLAT PANEL DETECTOR

K-Number: K121444 · 2012-06-07

ApplicantCanon, Inc. - Medical Equpment Group
Decision Date2012-06-07
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLAT PANEL DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc. - Medical Equpment Group. It received FDA 510(k) clearance on 2012-06-07 under 510(k) number K121444. 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 FLAT PANEL DETECTOR?

FLAT PANEL DETECTOR is a medical device that received FDA 510(k) clearance on 2012-06-07. The listed applicant is Canon, Inc. - Medical Equpment Group. The 510(k) number is K121444.

When did FLAT PANEL DETECTOR receive FDA 510(k) clearance?

FLAT PANEL DETECTOR received FDA 510(k) clearance on 2012-06-07, under 510(k) number K121444.

Who is the listed applicant for FLAT PANEL DETECTOR?

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

What is the FDA product code for FLAT PANEL DETECTOR?

The FDA product code for FLAT PANEL DETECTOR is OWB.

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Related Devices (Code: OWB)

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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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