VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK
K-Number: K992366 · 1999-10-08
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Device Summary
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.
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
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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