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FDA 510(k)

TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT

K-Number: K900167 · 1990-01-22

ApplicantBehring Diagnostics, Inc.
Decision Date1990-01-22
Product CodeDCF
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT 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 1990-01-22 under 510(k) number K900167. The device is classified under product code DCF. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT?

TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K900167.

When did TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT receive FDA 510(k) clearance?

TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT received FDA 510(k) clearance on 1990-01-22, under 510(k) number K900167.

Who is the listed applicant for TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT?

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 TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT?

The FDA product code for TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT is DCF.

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Related Devices (Code: DCF)

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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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