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FDA 510(k)

LOW PROFILE SAFSITE Y-SITE

K-Number: K954123 · 1995-11-21

ApplicantB.Braun Medical, Inc.
Decision Date1995-11-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOW PROFILE SAFSITE Y-SITE 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 1995-11-21 under 510(k) number K954123. 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 LOW PROFILE SAFSITE Y-SITE?

LOW PROFILE SAFSITE Y-SITE is a medical device that received FDA 510(k) clearance on 1995-11-21. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K954123.

When did LOW PROFILE SAFSITE Y-SITE receive FDA 510(k) clearance?

LOW PROFILE SAFSITE Y-SITE received FDA 510(k) clearance on 1995-11-21, under 510(k) number K954123.

Who is the listed applicant for LOW PROFILE SAFSITE Y-SITE?

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 LOW PROFILE SAFSITE Y-SITE?

The FDA product code for LOW PROFILE SAFSITE Y-SITE 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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