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FDA 510(k)

PIGGYBACK WIRE CONVERTER

K-Number: K090977 · 2009-06-18

ApplicantVascular Solutions, Inc.
Decision Date2009-06-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PIGGYBACK WIRE CONVERTER is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2009-06-18 under 510(k) number K090977. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIGGYBACK WIRE CONVERTER?

PIGGYBACK WIRE CONVERTER is a medical device that received FDA 510(k) clearance on 2009-06-18. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K090977.

When did PIGGYBACK WIRE CONVERTER receive FDA 510(k) clearance?

PIGGYBACK WIRE CONVERTER received FDA 510(k) clearance on 2009-06-18, under 510(k) number K090977.

Who is the listed applicant for PIGGYBACK WIRE CONVERTER?

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

What is the FDA product code for PIGGYBACK WIRE CONVERTER?

The FDA product code for PIGGYBACK WIRE CONVERTER is DQY.

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Other records listing Vascular Solutions, Inc. as applicant

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Related Devices (Code: DQY)

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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