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FDA 510(k)

RADIAL AND FEMORAL ARTERY CATHETER

K-Number: K971086 · 1997-12-19

ApplicantB.Braun Medical, Inc.
Decision Date1997-12-19
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RADIAL AND FEMORAL ARTERY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1997-12-19 under 510(k) number K971086. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIAL AND FEMORAL ARTERY CATHETER?

RADIAL AND FEMORAL ARTERY CATHETER is a medical device that received FDA 510(k) clearance on 1997-12-19. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K971086.

When did RADIAL AND FEMORAL ARTERY CATHETER receive FDA 510(k) clearance?

RADIAL AND FEMORAL ARTERY CATHETER received FDA 510(k) clearance on 1997-12-19, under 510(k) number K971086.

Who is the listed applicant for RADIAL AND FEMORAL ARTERY CATHETER?

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

What is the FDA product code for RADIAL AND FEMORAL ARTERY CATHETER?

The FDA product code for RADIAL AND FEMORAL ARTERY CATHETER is DQX.

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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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