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FDA 510(k)

QUANTICHECK CONTROL PLASMA

K-Number: K803081 · 1981-03-17

ApplicantAbbott Laboratories
Decision Date1981-03-17
Product CodeGGQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QUANTICHECK CONTROL PLASMA is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1981-03-17 under 510(k) number K803081. The device is classified under product code GGQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTICHECK CONTROL PLASMA?

QUANTICHECK CONTROL PLASMA is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Abbott Laboratories. The 510(k) number is K803081.

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

QUANTICHECK CONTROL PLASMA received FDA 510(k) clearance on 1981-03-17, under 510(k) number K803081.

Who is the listed applicant for QUANTICHECK CONTROL PLASMA?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTICHECK CONTROL PLASMA?

The FDA product code for QUANTICHECK CONTROL PLASMA is GGQ.

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Related Devices (Code: GGQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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