Atlas FDA

MOBILE C-ARM

FDA 510(k) clearance K121303 · decided 2012-07-26

Clearance details

K-number
K121303
Device name
MOBILE C-ARM
Applicant
Canon Inc. -Medical Equipment Group
Decision
Substantially Equivalent
Date received
2012-05-01
Decision date
2012-07-26
Days to decision
86 days
Clearance type
Traditional
Product code
OXO
Device class
2
Regulation number
892.1650
Medical specialty
Radiology
Advisory committee
Radiology
Location
Richardson, TX, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Canon Inc. -Medical Equipment Group

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Digital C-ARM with 3D (K253296)Allengers Medical Systems Limited2026-06-05
Orthoscan TAU MVP Mini C-Arm System (K252579)Ziehm-Orthoscan, Inc.2026-01-14
OEC One CFD (K253269)Ge Hualun Medical Systems Co. , Ltd.2025-11-26
Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M) (K251004)Hefei Chimed Intelligent Machine Co., Ltd.2025-11-06
Orthoscan TAU Mini C-Arm (K250587)Ziehm-Orthoscan, Inc.2025-07-02
Orthoscan VERSA Mini C-Arm (K243452)Ziehm-Orthoscan, Inc.2025-01-14
OEC One ASD (K240828)Ge Hualun Medical Systems Co. , Ltd.2024-12-27
OEC 3D (K233669)Ge Oec Medical Systems, Inc.2024-03-28
Orthoscan Tau Mini C-Arm (K213113)Orthoscan, Inc.2021-10-21
OEC 3D (K203346)Ge Oec Medical Systems, Inc.2021-03-05
OEC Elite (K192819)Ge Oec Medical Systems, Inc.2019-11-08
Smart-C (K190024)Turner Imaging Systems, Inc.2019-09-27

Recalls involving this device

No recalls on record reference this clearance.