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FDA 510(k)

MERIVIEW TM TRICHOMONAS

K-Number: K894246 · 1989-08-15

ApplicantMeridian Diagnostics, Inc.
Decision Date1989-08-15
Product CodeJWZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MERIVIEW TM TRICHOMONAS is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1989-08-15 under 510(k) number K894246. The device is classified under product code JWZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVIEW TM TRICHOMONAS?

MERIVIEW TM TRICHOMONAS is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K894246.

When did MERIVIEW TM TRICHOMONAS receive FDA 510(k) clearance?

MERIVIEW TM TRICHOMONAS received FDA 510(k) clearance on 1989-08-15, under 510(k) number K894246.

Who is the listed applicant for MERIVIEW TM TRICHOMONAS?

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

What is the FDA product code for MERIVIEW TM TRICHOMONAS?

The FDA product code for MERIVIEW TM TRICHOMONAS is JWZ.

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Other records listing Meridian Diagnostics, 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.

K993914PREMIER TOXINS A&B, MODEL 616096K990263IMMUNOCARD STAT! E. COLI O157:H7K984343PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TESTK984346PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TESTK983255MODIFICATION TO: PREMIER PLATINUM HPSAK982764PREMIER CRYPTOSPORIDIUM

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Related Devices (Code: JWZ)

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.

K033864GENZYME OSOM TRICHOMONAS RAPID TESTGenzyme Corp.K020595XENOSTRIP-TV TRICHOMONAS CASSETTE TEST, MODEL C1383.01Xenotope Diagnostics, Inc.K020226XENOSTRIP-TV TRICHOMONAS DIAGNOSTIC TEST KIT; CATALOG NUMBERS S1383.01, S1383.02 & S1383.03Hellen Professional ServicesK892802SUPER DUOMercia Diagnostics , Ltd.K892263MERIFLUOR(TM) -TRICHOMONASMeridian Diagnostics, Inc.K875138TRICHOMATE(R) SUPERMercia Diagnostics , Ltd.

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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