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FDA 510(k)

BURRON CARDIOVASCULAR ANGESTAT(TM)

K-Number: K931743 · 1993-11-02

ApplicantB.Braun Medical, Inc.
Decision Date1993-11-02
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BURRON CARDIOVASCULAR ANGESTAT(TM) 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 1993-11-02 under 510(k) number K931743. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURRON CARDIOVASCULAR ANGESTAT(TM)?

BURRON CARDIOVASCULAR ANGESTAT(TM) is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K931743.

When did BURRON CARDIOVASCULAR ANGESTAT(TM) receive FDA 510(k) clearance?

BURRON CARDIOVASCULAR ANGESTAT(TM) received FDA 510(k) clearance on 1993-11-02, under 510(k) number K931743.

Who is the listed applicant for BURRON CARDIOVASCULAR ANGESTAT(TM)?

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 BURRON CARDIOVASCULAR ANGESTAT(TM)?

The FDA product code for BURRON CARDIOVASCULAR ANGESTAT(TM) is DYB.

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Related Devices (Code: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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