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FDA 510(k)

SEEKER CROSSING SUPPORT CATHETER

K-Number: K103367 · 2010-12-08

ApplicantBard Peripheral Vascular, Inc.
Decision Date2010-12-08
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEEKER CROSSING SUPPORT CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2010-12-08 under 510(k) number K103367. 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 SEEKER CROSSING SUPPORT CATHETER?

SEEKER CROSSING SUPPORT CATHETER is a medical device that received FDA 510(k) clearance on 2010-12-08. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K103367.

When did SEEKER CROSSING SUPPORT CATHETER receive FDA 510(k) clearance?

SEEKER CROSSING SUPPORT CATHETER received FDA 510(k) clearance on 2010-12-08, under 510(k) number K103367.

Who is the listed applicant for SEEKER CROSSING SUPPORT CATHETER?

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

What is the FDA product code for SEEKER CROSSING SUPPORT CATHETER?

The FDA product code for SEEKER CROSSING SUPPORT CATHETER is DQY.

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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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