Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K821430Substantially Equivalent

Mueller Hinton Medium

Interstate Media, Mchenry IL / Traditional, Substantially Equivalent

K821430 is the FDA 510(k) clearance record for MUELLER HINTON MEDIUM, a class II device, cleared for Interstate Media on under FDA product code JTZ (Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth). FDA records list 15 510(k) clearances for Interstate Media. As of , FDA records show no recalls naming K821430.

Clearance record

Decision date
Received
(20 days to decision)
Product code
JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth
Regulation
21 CFR 866.1700
Device class
Class II
Review panel
Microbiology
Applicant
Interstate Media 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JTZ

Trailing 12 months
1 clearance under product code JTZ in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JTZ, 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 20261
October 20260