Cleared Traditional

K811608 - MUELLER-HINTON

K811608 is an FDA 510(k) clearance for MUELLER-HINTON, manufactured by Micro Media Laboratories. The device is a Class 2 Microbiology device with product code JTZ cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K811608 · Micro Media Laboratories · Microbiology device
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Jun 1981
Decision
17d
Days
Class 2
Risk

K811608 is an FDA 510(k) clearance for the MUELLER-HINTON. Classified as Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/broth (product code JTZ), Class II - Special Controls.

Submitted by Micro Media Laboratories (Mchenry, US). The FDA issued a Cleared decision on June 25, 1981 after a review of 17 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.1700 - the FDA microbiology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Micro Media Laboratories devices

FDA 510(k) Submission Details - K811608

510(k) Number K811608 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1981
Decision Date June 25, 1981
Days to Decision 17 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 102d · This submission: 17d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JTZ Device Classification - Class 2, Special Controls

Product Code JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/broth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.1700
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Microbiology devices follow this clearance model.

Regulatory Peers - JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/broth

All 44
Devices cleared under the same product code (JTZ) and FDA review panel - the closest regulatory comparables to K811608.
#1904L MUELLER HINTON W/5% SHEEP BLOOD
K820793 · Biomedica, Inc. · Apr 1982
#19012 CHOCOLATE MUELLER HINTON-150X15MM
K820794 · Biomedica, Inc. · Apr 1982
MUELLER HINTON AGAR
K811646 · Hardy Media · Jul 1981
MUELLER HINTON AGAR
K811471 · Biomedia, Inc. · Jun 1981
MUELLER HINTON AGAR, POURED INTO A PLATE
K811472 · Biomedia, Inc. · Jun 1981
MUELLER HINTON AGAR W/5% SHEEP BLOOD
K811473 · Biomedia, Inc. · Jun 1981