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FDA 510(k)

MERIFLUOR(TM)-GIARDIA

K-Number: K873299 · 1987-09-16

ApplicantMeridian Diagnostics, Inc.
Decision Date1987-09-16
Product CodeGWD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MERIFLUOR(TM)-GIARDIA 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 1987-09-16 under 510(k) number K873299. The device is classified under product code GWD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIFLUOR(TM)-GIARDIA?

MERIFLUOR(TM)-GIARDIA is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K873299.

When did MERIFLUOR(TM)-GIARDIA receive FDA 510(k) clearance?

MERIFLUOR(TM)-GIARDIA received FDA 510(k) clearance on 1987-09-16, under 510(k) number K873299.

Who is the listed applicant for MERIFLUOR(TM)-GIARDIA?

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 MERIFLUOR(TM)-GIARDIA?

The FDA product code for MERIFLUOR(TM)-GIARDIA is GWD.

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Other records listing Meridian Diagnostics, Inc. as applicant

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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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