510(k) K222652
K222652 is an FDA 510(k) premarket notification submitted by Cardicare Company, Ltd. for the device "Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer". The FDA issued a decision of Substantially Equivalent on November 28, 2022. The device falls under product code DXQ (Blood Pressure Cuff), a Class II device regulated under 21 CFR 870.1120. Cardicare Company, Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 28, 2022
- Date Received
- September 1, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Blood Pressure Cuff
- Device Class
- Class II
- Regulation Number
- 870.1120
- Review Panel
- CV
- Submission Type
A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure.