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FDA 510(k)

(MERIFLUOR)TM-CRYPTOSPORIDIUM

K-Number: K870171 · 1987-03-16

ApplicantMeridian Diagnostics, Inc.
Decision Date1987-03-16
Product Code
DecisionSubstantially Equivalent

Device Summary

(MERIFLUOR)TM-CRYPTOSPORIDIUM 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 1987-03-16 under 510(k) number K870171. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the (MERIFLUOR)TM-CRYPTOSPORIDIUM?

(MERIFLUOR)TM-CRYPTOSPORIDIUM is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K870171.

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

(MERIFLUOR)TM-CRYPTOSPORIDIUM received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870171.

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

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

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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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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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