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FDA 510(k)

CLIBRATION PLASMAS

K-Number: K924404 · 1992-12-01

ApplicantBehring Diagnostics, Inc.
Decision Date1992-12-01
Product CodeGGN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CLIBRATION PLASMAS 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 1992-12-01 under 510(k) number K924404. The device is classified under product code GGN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLIBRATION PLASMAS?

CLIBRATION PLASMAS is a medical device that received FDA 510(k) clearance on 1992-12-01. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K924404.

When did CLIBRATION PLASMAS receive FDA 510(k) clearance?

CLIBRATION PLASMAS received FDA 510(k) clearance on 1992-12-01, under 510(k) number K924404.

Who is the listed applicant for CLIBRATION PLASMAS?

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 CLIBRATION PLASMAS?

The FDA product code for CLIBRATION PLASMAS is GGN.

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Other records listing Behring Diagnostics, Inc. as applicant

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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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