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FDA 510(k)

ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG

K-Number: K073396 · 2008-08-07

ApplicantB.Braun Medical, Inc.
Decision Date2008-08-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG 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 2008-08-07 under 510(k) number K073396. 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 ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG?

ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG is a medical device that received FDA 510(k) clearance on 2008-08-07. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K073396.

When did ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG receive FDA 510(k) clearance?

ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG received FDA 510(k) clearance on 2008-08-07, under 510(k) number K073396.

Who is the listed applicant for ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG?

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 ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG?

The FDA product code for ANTIMICROBIAL ULTRASITE VALUE, ULTRASITE AG is 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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