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FDA 510(k)

QUINTON Q-CATH, MODEL 000460

K-Number: K021906 · 2002-09-04

ApplicantQuinton, Inc.
Decision Date2002-09-04
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUINTON Q-CATH, MODEL 000460 is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 2002-09-04 under 510(k) number K021906. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUINTON Q-CATH, MODEL 000460?

QUINTON Q-CATH, MODEL 000460 is a medical device that received FDA 510(k) clearance on 2002-09-04. The listed applicant is Quinton, Inc.. The 510(k) number is K021906.

When did QUINTON Q-CATH, MODEL 000460 receive FDA 510(k) clearance?

QUINTON Q-CATH, MODEL 000460 received FDA 510(k) clearance on 2002-09-04, under 510(k) number K021906.

Who is the listed applicant for QUINTON Q-CATH, MODEL 000460?

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

What is the FDA product code for QUINTON Q-CATH, MODEL 000460?

The FDA product code for QUINTON Q-CATH, MODEL 000460 is DQK.

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Other records listing Quinton, Inc. as applicant

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Related Devices (Code: DQK)

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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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