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FDA 510(k)

CONTRAST MEDIA TRANSFER SETS

K-Number: K052252 · 2005-11-16

ApplicantB.Braun Medical, Inc.
Decision Date2005-11-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTRAST MEDIA TRANSFER SETS 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 2005-11-16 under 510(k) number K052252. 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 CONTRAST MEDIA TRANSFER SETS?

CONTRAST MEDIA TRANSFER SETS is a medical device that received FDA 510(k) clearance on 2005-11-16. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K052252.

When did CONTRAST MEDIA TRANSFER SETS receive FDA 510(k) clearance?

CONTRAST MEDIA TRANSFER SETS received FDA 510(k) clearance on 2005-11-16, under 510(k) number K052252.

Who is the listed applicant for CONTRAST MEDIA TRANSFER SETS?

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 CONTRAST MEDIA TRANSFER SETS?

The FDA product code for CONTRAST MEDIA TRANSFER SETS is FPA.

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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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