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FDA 510(k)

IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING

K-Number: K041490 · 2004-10-29

ApplicantB.Braun Medical, Inc.
Decision Date2004-10-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING 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 2004-10-29 under 510(k) number K041490. 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 IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING?

IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING is a medical device that received FDA 510(k) clearance on 2004-10-29. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K041490.

When did IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING receive FDA 510(k) clearance?

IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING received FDA 510(k) clearance on 2004-10-29, under 510(k) number K041490.

Who is the listed applicant for IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING?

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 IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING?

The FDA product code for IV ADMINISTRATION SETS WITH ULTRABLOCK UV-RESISTANT TUBING is FPA.

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Related Devices (Code: FPA)

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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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