Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K952250Substantially Equivalent

Stratus Ck-Mb Dendrimer Fluorometric Enzyme Immunoassay & Stratus Ck-Mb Dendrimer High Sample Diluent

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

K952250 is the FDA 510(k) clearance record for STRATUS CK-MB DENDRIMER FLUOROMETRIC ENZYME IMMUNOASSAY & STRATUS CK-MB DENDRIMER HIGH SAMPLE DILUENT, a class II device, cleared for Dade Intl., Inc. on under FDA product code JHS (Differential Rate Kinetic Method, Cpk Or Isoenzymes). FDA records list 30 510(k) clearances for Dade Intl., Inc., from to . As of , FDA records show no recalls naming K952250.

Clearance record

Decision date
Received
(63 days to decision)
Product code
JHS Differential Rate Kinetic Method, Cpk Or Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Dade Intl., Inc. P.O.Box 520672, Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code JHS

Trailing 12 months

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

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