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FDA 510(k)

ECG BASED MEDIA

K-Number: K873267 · 1987-11-04

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

Device Summary

ECG BASED 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 K873267. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECG BASED MEDIA?

ECG BASED 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 K873267.

When did ECG BASED MEDIA receive FDA 510(k) clearance?

ECG BASED MEDIA received FDA 510(k) clearance on 1987-11-04, under 510(k) number K873267.

Who is the listed applicant for ECG BASED 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 ECG BASED MEDIA?

The FDA product code for ECG BASED MEDIA is KZI.

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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 MEDIAK873270ACTINOMYCETE DIFFERENTIAL MEDIAK873268MUELLER HINTON MEDIA

View all 14 devices →

Related Devices (Code: KZI)

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.

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880122MIDDLEBROOK 7H9 BROTHHardy MediaK880131LOWENSTEIN-JENSEN, GRUFTHardy MediaK880134MIDDLEBROOK 7H11 AGARHardy MediaK880138WALLENSTEIN MEDIUM SLANTHardy Media

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.

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