Angiography/Angioplasty Kit
The Angiography/Angioplasty Kit (product code OEQ) is a cardiovascular convenience kit assembled from components used in angiography or angioplasty procedures. It was established under the May 1997 FDA Convenience Kits Interim Regulatory Guidance and is under enforcement discretion, meaning it does not require a premarket notification (510(k)) to market provided it meets all criteria in that guidance. This device is FDA Class 2 under regulation 870.1650 in the Cardiovascular specialty. It carries no implant or life-sustaining flags.
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Basic Information
- Product Code
- OEQ
- Device Class
- FDA class 2
- Regulation Number
- 870.1650
- Medical Specialty
- Cardiovascular
- Review Panel
- CV
- Submission Type
- 7
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 www.Fda.Gov/cdrh/ode/convkit.Html. 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 52 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 52 registration numbers. Click on an entry to view related FDA registrations.