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FDA 510(k)

BRAUN HEMODIALYSIS BLOOD CIRCUITS

K-Number: K952631 · 1996-04-30

ApplicantB.Braun Medical, Inc.
Decision Date1996-04-30
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BRAUN HEMODIALYSIS BLOOD CIRCUITS 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 1996-04-30 under 510(k) number K952631. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAUN HEMODIALYSIS BLOOD CIRCUITS?

BRAUN HEMODIALYSIS BLOOD CIRCUITS is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K952631.

When did BRAUN HEMODIALYSIS BLOOD CIRCUITS receive FDA 510(k) clearance?

BRAUN HEMODIALYSIS BLOOD CIRCUITS received FDA 510(k) clearance on 1996-04-30, under 510(k) number K952631.

Who is the listed applicant for BRAUN HEMODIALYSIS BLOOD CIRCUITS?

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 BRAUN HEMODIALYSIS BLOOD CIRCUITS?

The FDA product code for BRAUN HEMODIALYSIS BLOOD CIRCUITS is FJK.

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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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