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FDA 510(k)

V3 VALVE

K-Number: K974145 · 1998-01-06

ApplicantB.Braun Medical, Inc.
Decision Date1998-01-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V3 VALVE 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 1998-01-06 under 510(k) number K974145. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V3 VALVE?

V3 VALVE is a medical device that received FDA 510(k) clearance on 1998-01-06. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K974145.

When did V3 VALVE receive FDA 510(k) clearance?

V3 VALVE received FDA 510(k) clearance on 1998-01-06, under 510(k) number K974145.

Who is the listed applicant for V3 VALVE?

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 V3 VALVE?

The FDA product code for V3 VALVE is FPA.

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Other records listing B.Braun Medical, Inc. as applicant

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Related Devices (Code: FPA)

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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