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FDA 510(k)

PROTEIN S AC

K-Number: K022290 · 2002-08-27

ApplicantDade Behring, Inc.
Decision Date2002-08-27
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PROTEIN S AC is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2002-08-27 under 510(k) number K022290. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTEIN S AC?

PROTEIN S AC is a medical device that received FDA 510(k) clearance on 2002-08-27. The listed applicant is Dade Behring, Inc.. The 510(k) number is K022290.

When did PROTEIN S AC receive FDA 510(k) clearance?

PROTEIN S AC received FDA 510(k) clearance on 2002-08-27, under 510(k) number K022290.

Who is the listed applicant for PROTEIN S AC?

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

What is the FDA product code for PROTEIN S AC?

The FDA product code for PROTEIN S AC is GGP.

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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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