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FDA 510(k)

LIQUICHEK D-DIMER CONTROL, MODEL 356, 357

K-Number: K030182 · 2003-02-24

ApplicantBio-Rad
Decision Date2003-02-24
Product CodeGGN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK D-DIMER CONTROL, MODEL 356, 357 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 2003-02-24 under 510(k) number K030182. 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 LIQUICHEK D-DIMER CONTROL, MODEL 356, 357?

LIQUICHEK D-DIMER CONTROL, MODEL 356, 357 is a medical device that received FDA 510(k) clearance on 2003-02-24. The listed applicant is Bio-Rad. The 510(k) number is K030182.

When did LIQUICHEK D-DIMER CONTROL, MODEL 356, 357 receive FDA 510(k) clearance?

LIQUICHEK D-DIMER CONTROL, MODEL 356, 357 received FDA 510(k) clearance on 2003-02-24, under 510(k) number K030182.

Who is the listed applicant for LIQUICHEK D-DIMER CONTROL, MODEL 356, 357?

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

What is the FDA product code for LIQUICHEK D-DIMER CONTROL, MODEL 356, 357?

The FDA product code for LIQUICHEK D-DIMER CONTROL, MODEL 356, 357 is GGN.

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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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