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FDA 510(k)

TURBIQUANT

K-Number: K920124 · 1992-03-02

ApplicantBehring Diagnostics, Inc.
Decision Date1992-03-02
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TURBIQUANT 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 1992-03-02 under 510(k) number K920124. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBIQUANT?

TURBIQUANT is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K920124.

When did TURBIQUANT receive FDA 510(k) clearance?

TURBIQUANT received FDA 510(k) clearance on 1992-03-02, under 510(k) number K920124.

Who is the listed applicant for TURBIQUANT?

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?

The FDA product code for TURBIQUANT is DHR.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: DHR)

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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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