510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K092604Substantially Equivalent

Large Face Aneroid Sphygmomanometer, Wall Model, Desk Model, Mobile Stand Model, Model 41Xx, 42Xx, 43Xx

Trimline Medical Products Corp., Branchburg NJ / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092604 is the FDA 510(k) clearance record for LARGE FACE ANEROID SPHYGMOMANOMETER, WALL MODEL, DESK MODEL, MOBILE STAND MODEL, MODEL 41XX, 42XX, 43XX, a class II device, cleared for Trimline Medical Products Corp. 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 Trimline Medical Products Corp., from to . As of , FDA records show no recalls naming K092604.

Clearance record

Decision date
Received
(57 days to decision)
Product code
DXQ Blood Pressure Cuff
Regulation
21 CFR 870.1120
Device class
Class II
Review panel
Cardiovascular
Applicant
Trimline Medical Products Corp. 34 Columbia Ave., Branchburg NJ
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