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FDA 510(k)

MOBILE C-ARM

K-Number: K121303 · 2012-07-26

Decision Date2012-07-26
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILE C-ARM is the device name listed in this FDA 510(k) record. The listed applicant is Canon Inc. -Medical Equipment Group. It received FDA 510(k) clearance on 2012-07-26 under 510(k) number K121303. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILE C-ARM?

MOBILE C-ARM is a medical device that received FDA 510(k) clearance on 2012-07-26. The listed applicant is Canon Inc. -Medical Equipment Group. The 510(k) number is K121303.

When did MOBILE C-ARM receive FDA 510(k) clearance?

MOBILE C-ARM received FDA 510(k) clearance on 2012-07-26, under 510(k) number K121303.

Who is the listed applicant for MOBILE C-ARM?

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

What is the FDA product code for MOBILE C-ARM?

The FDA product code for MOBILE C-ARM is OXO.

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.

Other records listing Canon Inc. -Medical Equipment Group 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.

View all 11 devices →

Related Devices (Code: OXO)

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.

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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