FDA 510(k)

BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS

K-Number: K955485 · 1996-02-23

Decision Date1996-02-23

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS 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 1996-02-23 under 510(k) number K955485. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS?

BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1996-02-23. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K955485.

When did BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1996-02-23, under 510(k) number K955485.

Who is the listed applicant for BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS?

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 BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS?

The FDA product code for BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.