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FDA 510(k)

ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET

K-Number: K930057 · 1993-08-06

ApplicantB.Braun Medical, Inc.
Decision Date1993-08-06
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET 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 1993-08-06 under 510(k) number K930057. 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 ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET?

ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K930057.

When did ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET receive FDA 510(k) clearance?

ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET received FDA 510(k) clearance on 1993-08-06, under 510(k) number K930057.

Who is the listed applicant for ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET?

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 ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET?

The FDA product code for ANGESTAT FLUORO-TIP HEMOSTASIS INTRODUCER SET 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.

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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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