Medical Device
Manufacturing
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K964862Substantially Equivalent

Troponin-I Test System

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

K964862 is the FDA 510(k) clearance record for TROPONIN-I TEST SYSTEM, a class II device, cleared for Dade Intl., Inc. on under FDA product code MMI (Immunoassay Method, Troponin Subunit). FDA records list 30 510(k) clearances for Dade Intl., Inc., from to . As of , FDA records show no recalls naming K964862.

Clearance record

Decision date
Received
(68 days to decision)
Product code
MMI Immunoassay Method, Troponin Subunit
Regulation
21 CFR 862.1215
Device class
Class II
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 MMI

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