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FDA 510(k)

MAHURKAR DUAL LIMEN FEMORAL CATHETER

K-Number: K834109 · 1984-02-04

ApplicantQuinton, Inc.
Decision Date1984-02-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAHURKAR DUAL LIMEN FEMORAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K834109. 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 MAHURKAR DUAL LIMEN FEMORAL CATHETER?

MAHURKAR DUAL LIMEN FEMORAL CATHETER is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Quinton, Inc.. The 510(k) number is K834109.

When did MAHURKAR DUAL LIMEN FEMORAL CATHETER receive FDA 510(k) clearance?

MAHURKAR DUAL LIMEN FEMORAL CATHETER received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834109.

Who is the listed applicant for MAHURKAR DUAL LIMEN FEMORAL CATHETER?

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 MAHURKAR DUAL LIMEN FEMORAL CATHETER?

The FDA product code for MAHURKAR DUAL LIMEN FEMORAL CATHETER is DQY.

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Other records listing Quinton, 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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