510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K222652Substantially Equivalent

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer

Cardicare Company, Ltd., Hangzhou City, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222652 is the FDA 510(k) clearance record for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer, a class II device, cleared for Cardicare Company, Ltd. on under FDA product code DXQ (Blood Pressure Cuff). FDA's definition for product code DXQ reads: "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". FDA records list 2 510(k) clearances for Cardicare Company, Ltd., from to . As of , FDA records show no recalls naming K222652.

Clearance record

Decision date
Received
(88 days to decision)
Product code
DXQ Blood Pressure Cuff
Regulation
21 CFR 870.1120
Device class
Class II
Review panel
Cardiovascular
Applicant
Cardicare Company, Ltd. 9 Yan An Rd., Wu Shan Plz. Town, Unit 7003, Hangzhou City, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXQ

Trailing 12 months
5 clearances under product code DXQ in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXQ, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260