FDA 510(k)

CELSITE PEDIATRIC VENOUS SYSTEM

K-Number: K952435 · 1996-04-17

Decision Date1996-04-17

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CELSITE PEDIATRIC VENOUS SYSTEM 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 1996-04-17 under 510(k) number K952435. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELSITE PEDIATRIC VENOUS SYSTEM?

CELSITE PEDIATRIC VENOUS SYSTEM is a medical device that received FDA 510(k) clearance on 1996-04-17. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K952435.

When did CELSITE PEDIATRIC VENOUS SYSTEM receive FDA 510(k) clearance?

CELSITE PEDIATRIC VENOUS SYSTEM received FDA 510(k) clearance on 1996-04-17, under 510(k) number K952435.

Who is the listed applicant for CELSITE PEDIATRIC VENOUS SYSTEM?

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 CELSITE PEDIATRIC VENOUS SYSTEM?

The FDA product code for CELSITE PEDIATRIC VENOUS SYSTEM is LJT.

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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.