Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K973974Substantially Equivalent

Dade Tru-Liquid Cardiac Control

Dade Intl., Inc., Miami FL / Traditional, Substantially Equivalent

K973974 is the FDA 510(k) clearance record for DADE TRU-LIQUID CARDIAC CONTROL, a class I device, cleared for Dade Intl., Inc. on under FDA product code JJT (Enzyme Controls (Assayed And Unassayed)). FDA records list 30 510(k) clearances for Dade Intl., Inc., from to . As of , FDA records show no recalls naming K973974.

Clearance record

Decision date
Received
(17 days to decision)
Product code
JJT Enzyme Controls (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Dade Intl., Inc. 2173 NW 99th Ave., Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code JJT

Trailing 12 months

FDA records hold no clearances under product code JJT in the trailing twelve months.

FDA records show no clearances under product code JJT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JJT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260