510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K974080Substantially Equivalent

Critikon Soft Blood Pressure Cuff

Johnson & Johnson MEDICAL GmbH, Tampa FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974080 is the FDA 510(k) clearance record for CRITIKON SOFT BLOOD PRESSURE CUFF, a class II device, cleared for Johnson & Johnson Medical, Inc. 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 56 510(k) clearances for Johnson & Johnson Medical, Inc., from to . As of , FDA records show one recall naming K974080.

Clearance record

Decision date
Received
(201 days to decision)
Product code
DXQ Blood Pressure Cuff
Regulation
21 CFR 870.1120
Device class
Class II
Review panel
Cardiovascular
Applicant
Johnson & Johnson Medical, Inc. 4110 George Rd., Tampa FL
510(k) summary
Summary
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