510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873656Substantially Equivalent

Medatron Cuvette Disc

Medatron, Inc., Brookfield WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873656 is the FDA 510(k) clearance record for MEDATRON CUVETTE DISC, a class I device, cleared for Medatron, Inc. on under FDA product code JRI (Cuvette, Thermostated). FDA records list one 510(k) clearance for Medatron, Inc. As of , FDA records show no recalls naming K873656.

Clearance record

Decision date
Received
(95 days to decision)
Product code
JRI Cuvette, Thermostated
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Medatron, Inc. C/O Professional Billing Co., Brookfield WI
Third party review
No

Clearances, product code JRI

Trailing 12 months

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

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