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FDA 510(k)

VGF-7 VASCULAR GRAFT FLOWMETER

K-Number: K973198 · 1998-10-14

ApplicantMedicard , Ltd.
Decision Date1998-10-14
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VGF-7 VASCULAR GRAFT FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medicard , Ltd.. It received FDA 510(k) clearance on 1998-10-14 under 510(k) number K973198. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VGF-7 VASCULAR GRAFT FLOWMETER?

VGF-7 VASCULAR GRAFT FLOWMETER is a medical device that received FDA 510(k) clearance on 1998-10-14. The listed applicant is Medicard , Ltd.. The 510(k) number is K973198.

When did VGF-7 VASCULAR GRAFT FLOWMETER receive FDA 510(k) clearance?

VGF-7 VASCULAR GRAFT FLOWMETER received FDA 510(k) clearance on 1998-10-14, under 510(k) number K973198.

Who is the listed applicant for VGF-7 VASCULAR GRAFT FLOWMETER?

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

What is the FDA product code for VGF-7 VASCULAR GRAFT FLOWMETER?

The FDA product code for VGF-7 VASCULAR GRAFT FLOWMETER is DPW.

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Official Source

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