Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MUELLER HINTON MEDIA

K-Number: K873268 · 1987-11-04

ApplicantCentral Media
Decision Date1987-11-04
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Central Media. It received FDA 510(k) clearance on 1987-11-04 under 510(k) number K873268. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUELLER HINTON MEDIA?

MUELLER HINTON MEDIA is a medical device that received FDA 510(k) clearance on 1987-11-04. The listed applicant is Central Media. The 510(k) number is K873268.

When did MUELLER HINTON MEDIA receive FDA 510(k) clearance?

MUELLER HINTON MEDIA received FDA 510(k) clearance on 1987-11-04, under 510(k) number K873268.

Who is the listed applicant for MUELLER HINTON MEDIA?

The FDA 510(k) record lists Central Media as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUELLER HINTON MEDIA?

The FDA product code for MUELLER HINTON MEDIA is JTZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Central Media as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K873259SPECIALTY MEDIAK873258STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIAK873257GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.K873260CORYNEBACTERIA ISOLATION MEDIAK873267ECG BASED MEDIAK873270ACTINOMYCETE DIFFERENTIAL MEDIA

View all 14 devices →

Related Devices (Code: JTZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262163BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton BrothBecton Dickinson and CompanyK963036MUELLER HINTON II BROTH (CATION-ADJUSTED) WITH LYSED HORSE BLOODBecton Dickinson Microbiology SystemsK960420MUELLER HINTON AGAR WITH 5% SHEEP BLOODBecton Dickinson Microbiology SystemsK960313MUELLER HINTON AGAR WITH 2% NACIRemel, L.P.K945911CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARSBioclinical Systems, Inc.K941985MUELLER HINTON AGAR W/OXACILLINCarr-Scarborough Microbiologicals, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑