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FDA 510(k)

VWF-IX:AG CONTROL PLASMA

K-Number: K861217 · 1986-05-20

ApplicantAmerican Bioproducts Co.
Decision Date1986-05-20
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VWF-IX:AG CONTROL PLASMA is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1986-05-20 under 510(k) number K861217. 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 VWF-IX:AG CONTROL PLASMA?

VWF-IX:AG CONTROL PLASMA is a medical device that received FDA 510(k) clearance on 1986-05-20. The listed applicant is American Bioproducts Co.. The 510(k) number is K861217.

When did VWF-IX:AG CONTROL PLASMA receive FDA 510(k) clearance?

VWF-IX:AG CONTROL PLASMA received FDA 510(k) clearance on 1986-05-20, under 510(k) number K861217.

Who is the listed applicant for VWF-IX:AG CONTROL PLASMA?

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

What is the FDA product code for VWF-IX:AG CONTROL PLASMA?

The FDA product code for VWF-IX:AG CONTROL PLASMA 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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