Arthrogram Tray
The Arthrogram Tray is a convenience kit providing the components needed to perform an arthrogram procedure, in which contrast material is injected into a joint under imaging guidance to evaluate joint structures such as cartilage, ligaments, and tendons. Classified as FDA Class 2 under regulation 21 CFR 892.1650 within the Radiology medical specialty, it is under enforcement discretion per the FDA's May 1997 Convenience Kits Interim Regulatory Guidance and does not require a 510(k) when all criteria are satisfied. The product code is OII. It is not flagged as an implant or life-sustaining device.
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Basic Information
- Product Code
- OII
- Device Class
- FDA class 2
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Review Panel
- RA
- Submission Type
- 4
Device Characteristics
Definition
This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
FEI Numbers
This FDA classification entry is associated with 18 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 18 registration numbers. Click on an entry to view related FDA registrations.