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FDA 510(k)

VON WILLEBRAND FACTOR ASSAY

K-Number: K802356 · 1980-12-01

ApplicantBio/Data Corp.
Decision Date1980-12-01
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VON WILLEBRAND FACTOR ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Bio/Data Corp.. It received FDA 510(k) clearance on 1980-12-01 under 510(k) number K802356. 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 VON WILLEBRAND FACTOR ASSAY?

VON WILLEBRAND FACTOR ASSAY is a medical device that received FDA 510(k) clearance on 1980-12-01. The listed applicant is Bio/Data Corp.. The 510(k) number is K802356.

When did VON WILLEBRAND FACTOR ASSAY receive FDA 510(k) clearance?

VON WILLEBRAND FACTOR ASSAY received FDA 510(k) clearance on 1980-12-01, under 510(k) number K802356.

Who is the listed applicant for VON WILLEBRAND FACTOR ASSAY?

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

What is the FDA product code for VON WILLEBRAND FACTOR ASSAY?

The FDA product code for VON WILLEBRAND FACTOR ASSAY is GGP.

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Other records listing Bio/Data Corp. as applicant

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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Related Devices (Code: 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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