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FDA 510(k)

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS

K-Number: K003112 · 2000-11-02

ApplicantOrtho-Clinical Diagnostics, Inc.
Decision Date2000-11-02
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS 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 2000-11-02 under 510(k) number K003112. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS?

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS is a medical device that received FDA 510(k) clearance on 2000-11-02. The listed applicant is Ortho-Clinical Diagnostics, Inc.. The 510(k) number is K003112.

When did VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS receive FDA 510(k) clearance?

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS received FDA 510(k) clearance on 2000-11-02, under 510(k) number K003112.

Who is the listed applicant for VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS?

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 ANTI-HBS CONTROLS?

The FDA product code for VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBS CONTROLS is JJX.

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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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