FDA 510(k)

SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER

K-Number: K971085 · 1997-06-02

Decision Date1997-06-02

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER 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 1997-06-02 under 510(k) number K971085. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER?

SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1997-06-02. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K971085.

When did SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1997-06-02, under 510(k) number K971085.

Who is the listed applicant for SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER?

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 SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER?

The FDA product code for SOFT TIP MULTI-LUMEN CENTRAL VENOUS CATHETER is LJS.

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Related Devices (Code: LJS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.