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FDA 510(k)

VWF IMMUNOBLOT

K-Number: K864701 · 1987-03-30

ApplicantRamco Laboratories, Inc.
Decision Date1987-03-30
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VWF IMMUNOBLOT is the device name listed in this FDA 510(k) record. The listed applicant is Ramco Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-30 under 510(k) number K864701. 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 IMMUNOBLOT?

VWF IMMUNOBLOT is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Ramco Laboratories, Inc.. The 510(k) number is K864701.

When did VWF IMMUNOBLOT receive FDA 510(k) clearance?

VWF IMMUNOBLOT received FDA 510(k) clearance on 1987-03-30, under 510(k) number K864701.

Who is the listed applicant for VWF IMMUNOBLOT?

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

What is the FDA product code for VWF IMMUNOBLOT?

The FDA product code for VWF IMMUNOBLOT is GGP.

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Other records listing Ramco Laboratories, Inc. as applicant

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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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