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FDA 510(k)

BRANNON ARTERIO-VENOUS PORTSYRINGE

K-Number: K965030 · 1997-03-04

ApplicantVascular Logics, Inc.
Decision Date1997-03-04
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BRANNON ARTERIO-VENOUS PORTSYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Logics, Inc.. It received FDA 510(k) clearance on 1997-03-04 under 510(k) number K965030. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANNON ARTERIO-VENOUS PORTSYRINGE?

BRANNON ARTERIO-VENOUS PORTSYRINGE is a medical device that received FDA 510(k) clearance on 1997-03-04. The listed applicant is Vascular Logics, Inc.. The 510(k) number is K965030.

When did BRANNON ARTERIO-VENOUS PORTSYRINGE receive FDA 510(k) clearance?

BRANNON ARTERIO-VENOUS PORTSYRINGE received FDA 510(k) clearance on 1997-03-04, under 510(k) number K965030.

Who is the listed applicant for BRANNON ARTERIO-VENOUS PORTSYRINGE?

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

What is the FDA product code for BRANNON ARTERIO-VENOUS PORTSYRINGE?

The FDA product code for BRANNON ARTERIO-VENOUS PORTSYRINGE is FMF.

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Related Devices (Code: FMF)

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

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

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