510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974343Substantially Equivalent

Dade Innovin

Dade Intl., Inc., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974343 is the FDA 510(k) clearance record for DADE INNOVIN, a class II device, cleared for Dade Intl., Inc. on under FDA product code GJS (Test, Time, Prothrombin). FDA records list 30 510(k) clearances for Dade Intl., Inc., from to . As of , FDA records show no recalls naming K974343.

Clearance record

Decision date
Received
(245 days to decision)
Product code
GJS Test, Time, Prothrombin
Regulation
21 CFR 864.7750
Device class
Class II
Review panel
Hematology
Applicant
Dade Intl., Inc. 2173 NW 99th Ave., Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code GJS

Trailing 12 months

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

FDA records show no clearances under product code GJS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GJS, 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