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FDA 510(k)

VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT

K-Number: K842617 · 1984-10-01

ApplicantAmerican Dade
Decision Date1984-10-01
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT is the device name listed in this FDA 510(k) record. The listed applicant is American Dade. It received FDA 510(k) clearance on 1984-10-01 under 510(k) number K842617. 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 VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT?

VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT is a medical device that received FDA 510(k) clearance on 1984-10-01. The listed applicant is American Dade. The 510(k) number is K842617.

When did VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT receive FDA 510(k) clearance?

VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT received FDA 510(k) clearance on 1984-10-01, under 510(k) number K842617.

Who is the listed applicant for VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT?

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

What is the FDA product code for VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT?

The FDA product code for VONWILLEBRAND FACTOR ANTIGEN SEMI-QUANT is GGP.

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Related Devices (Code: GGP)

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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