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FDA 510(k)

ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)

K-Number: K962745 · 1996-10-02

ApplicantPrepared Media Laboratory, Inc.
Decision Date1996-10-02
Product CodeJSN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000) is the device name listed in this FDA 510(k) record. The listed applicant is Prepared Media Laboratory, Inc.. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K962745. The device is classified under product code JSN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)?

ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000) is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Prepared Media Laboratory, Inc.. The 510(k) number is K962745.

When did ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000) receive FDA 510(k) clearance?

ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000) received FDA 510(k) clearance on 1996-10-02, under 510(k) number K962745.

Who is the listed applicant for ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)?

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

What is the FDA product code for ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)?

The FDA product code for ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000) is JSN.

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 Prepared Media Laboratory, Inc. 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.

K962744HAEMOPHILUS TEST MEDIUM AGAR (HTM)K782117MARTIN-LEWIS MEDIUM

Related Devices (Code: JSN)

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.

K000718CHROMOSTREAKNovamed , Ltd.K961755CYTOQUANT CHLAMYDIA TRANSPORT MEDIUMProteins Intl., Inc.K961756CYTOQUANT VIRAL TRANSPORT MEDIUMProteins Intl., Inc.K896296INPOUCH-TV POUCHBiomed Diagnostics, Inc.K881579AMIES TRANSPORT MEDIUM W/O CHARCOALAcumedia Manufacturers, Inc.K860967VIRTRAN VIRAL TRANSPORTER (MODIFIED)Diagnon Corp.

Official Source

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

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