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FDA 510(k)

CONTRAST MEDIA SET

K-Number: K955179 · 1997-03-12

ApplicantB.Braun Medical, Inc.
Decision Date1997-03-12
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONTRAST MEDIA SET 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 1997-03-12 under 510(k) number K955179. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTRAST MEDIA SET?

CONTRAST MEDIA SET is a medical device that received FDA 510(k) clearance on 1997-03-12. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K955179.

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

CONTRAST MEDIA SET received FDA 510(k) clearance on 1997-03-12, under 510(k) number K955179.

Who is the listed applicant for CONTRAST MEDIA SET?

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 SET?

The FDA product code for CONTRAST MEDIA SET is IZI.

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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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