FDA 510(k)

PERIPHERALLY INSERTED CENTRAL

K-Number: K971999 · 1997-11-24

Decision Date1997-11-24

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PERIPHERALLY INSERTED CENTRAL 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 1997-11-24 under 510(k) number K971999. 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 PERIPHERALLY INSERTED CENTRAL?

PERIPHERALLY INSERTED CENTRAL is a medical device that received FDA 510(k) clearance on 1997-11-24. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K971999.

When did PERIPHERALLY INSERTED CENTRAL receive FDA 510(k) clearance?

PERIPHERALLY INSERTED CENTRAL received FDA 510(k) clearance on 1997-11-24, under 510(k) number K971999.

Who is the listed applicant for PERIPHERALLY INSERTED CENTRAL?

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 PERIPHERALLY INSERTED CENTRAL?

The FDA product code for PERIPHERALLY INSERTED CENTRAL is 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.