FDA 510(k)

CONTROL PLASMA U

K-Number: K924402 · 1994-02-22

Decision Date1994-02-22

Product CodeGGC

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

CONTROL PLASMA U 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 1994-02-22 under 510(k) number K924402. The device is classified under product code GGC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROL PLASMA U?

CONTROL PLASMA U is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K924402.

When did CONTROL PLASMA U receive FDA 510(k) clearance?

CONTROL PLASMA U received FDA 510(k) clearance on 1994-02-22, under 510(k) number K924402.

Who is the listed applicant for CONTROL PLASMA U?

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 CONTROL PLASMA U?

The FDA product code for CONTROL PLASMA U is GGC.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: GGC)

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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.