510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K901506Substantially Equivalent

Aneroid Sphygmomanometer, Doctor Type

Yamasu Co., Ltd., Saitama Pref., JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901506 is the FDA 510(k) clearance record for ANEROID SPHYGMOMANOMETER, DOCTOR TYPE, a class II device, cleared for Yamasu Co. , 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 Yamasu Co. , Ltd., from to . As of , FDA records show no recalls naming K901506.

Clearance record

Decision date
Received
(40 days to decision)
Product code
DXQ Blood Pressure Cuff
Regulation
21 CFR 870.1120
Device class
Class II
Review panel
Cardiovascular
Applicant
Yamasu Co. , Ltd. 100 Nukui Kamikawa Mura, Saitama Pref., JP
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