Chocolate Mueller Hinton Agar

FDA 510(k) K871097 · bioMerieux, Inc.

Substantially Equivalent

510(k) numberK871097

Submission

Device name
Chocolate Mueller Hinton Agar
Applicant
bioMerieux, Inc.
Addison, IL, US
Received
March 18, 1987
Decision date
April 3, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JTZ – Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1700
Specialty
Microbiology

Other 510(k)s with product code JTZ

510(k)DeviceApplicantDecision
K132491Mueller Hinton AgarJTZ · Traditional Edge Biologicals, Inc.06/30/2014SE
K963036Mueller Hinton II Broth (Cation-Adjusted) with Lysed Horse BloodJTZ · Traditional Becton Dickinson Microbiology Systems10/07/1996SE
K960420Mueller Hinton Agar with 5% Sheep BloodJTZ · Traditional Becton Dickinson Microbiology Systems04/04/1996SE
K960313Mueller Hinton Agar with 2% NaciJTZ · Traditional Remel, L.P.03/25/1996SE
K945911Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton AgarsJTZ · Traditional Bioclinical Systems, Inc.04/04/1995SE
K941985Mueller Hinton Agar W/OxacillinJTZ · Traditional Carr-Scarborough Microbiologicals, Inc.08/24/1994SE
K882351Mueller Hinton Agar Plates P3318/1&2/P3418/P34181JTZ · Traditional Lakewood Biochemical Co., Inc.06/28/1988SE
K880105Muller Hinton BrothJTZ · Traditional Hardy Media03/30/1988SE
K873268Mueller Hinton MediaJTZ · Traditional Central Media11/04/1987SE
K870649Mrsa Screen Agar (Mueller Hinton W/Nacl & Oxacil.)JTZ · Traditional Hardy Media04/14/1987SE

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Questions and answers

When was Chocolate Mueller Hinton Agar cleared by the FDA?

Chocolate Mueller Hinton Agar (K871097) received a 510(k) decision of Substantially Equivalent on April 3, 1987, 16 days after the submission was received.

What is the product code of K871097?

The FDA product code is JTZ – Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth, a Class II (moderate risk) device regulated under 21 CFR 866.1700.