C-Arm Ceiling Crane FT-2
FDA 510(k) K840225 · Medicor USA , Ltd.
510(k) numberK840225
Submission
- Device name
- C-Arm Ceiling Crane FT-2
- Applicant
- Medicor USA , Ltd.
Mchenry, IL, US - Received
- January 19, 1984
- Decision date
- March 22, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was C-Arm Ceiling Crane FT-2 cleared by the FDA?
C-Arm Ceiling Crane FT-2 (K840225) received a 510(k) decision of Substantially Equivalent on March 22, 1984, 63 days after the submission was received.
What is the product code of K840225?
The FDA product code is JAA – System, X-Ray, Fluoroscopic, Image-Intensified, a Class II (moderate risk) device regulated under 21 CFR 892.1650.