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FDA 510(k)

VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK

K-Number: K992366 · 1999-10-08

Decision Date1999-10-08
Product CodeMMI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK is the device name listed in this FDA 510(k) record. The listed applicant is Ortho-Clinical Diagnostics, Inc.. It received FDA 510(k) clearance on 1999-10-08 under 510(k) number K992366. The device is classified under product code MMI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK?

VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK is a medical device that received FDA 510(k) clearance on 1999-10-08. The listed applicant is Ortho-Clinical Diagnostics, Inc.. The 510(k) number is K992366.

When did VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK receive FDA 510(k) clearance?

VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK received FDA 510(k) clearance on 1999-10-08, under 510(k) number K992366.

Who is the listed applicant for VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK?

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

What is the FDA product code for VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK?

The FDA product code for VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK is MMI.

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.

Other records listing Ortho-Clinical 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.

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Related Devices (Code: MMI)

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.

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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