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FDA 510(k)

MULTIFIBREN

K-Number: K925988 · 1993-03-01

ApplicantBehring Diagnostics, Inc.
Decision Date1993-03-01
Product CodeKQJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MULTIFIBREN is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1993-03-01 under 510(k) number K925988. The device is classified under product code KQJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIFIBREN?

MULTIFIBREN is a medical device that received FDA 510(k) clearance on 1993-03-01. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K925988.

When did MULTIFIBREN receive FDA 510(k) clearance?

MULTIFIBREN received FDA 510(k) clearance on 1993-03-01, under 510(k) number K925988.

Who is the listed applicant for MULTIFIBREN?

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

What is the FDA product code for MULTIFIBREN?

The FDA product code for MULTIFIBREN is KQJ.

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Other records listing Behring 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.

K973832OPUS HLH CONTROLSK972929N ANTISERUM TO HUMAN ALBUMINK972840N ANTISERUM TO HUMAN TRANSFERRINK973202MODIFICATION OF OPUS FERRITIN TEST SYSTEMK972316OPUS D-DIMERK972116VON WILLEBRAND REAGENT

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Related Devices (Code: KQJ)

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.

K251968HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XLInstrumentation Laboratory (IL) Co.K073367HEMOSIL FIBRINOGEN-CInstrumentation Laboratory COK050928DADE THROMBIN REAGENTDade Behring, Inc.K971858SIGMA DIAGNOSTICS FIBRINOGEN KIT (886A/887A)Sigma Diagnostics, Inc.K970189FIF TMPanbio, Inc.K965113N-ASSAY TIA FIBRINOGEN TEST KITCrestat Diagnostics, Inc.

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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