FDA 510(k)

SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20

K-Number: K992424 · 2000-12-29

ApplicantPlastimed Laboratoire Pharmaceutique

Decision Date2000-12-29

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20 is the device name listed in this FDA 510(k) record. The listed applicant is Plastimed Laboratoire Pharmaceutique. It received FDA 510(k) clearance on 2000-12-29 under 510(k) number K992424. 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 SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20?

SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20 is a medical device that received FDA 510(k) clearance on 2000-12-29. The listed applicant is Plastimed Laboratoire Pharmaceutique. The 510(k) number is K992424.

When did SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20 receive FDA 510(k) clearance?

SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20 received FDA 510(k) clearance on 2000-12-29, under 510(k) number K992424.

Who is the listed applicant for SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20?

The FDA 510(k) record lists Plastimed Laboratoire Pharmaceutique as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20?

The FDA product code for SELDIFLEX LONG-TERM CENTRAL VENOUS CATHETER(40CM & 60CM IN LENGTH), MODELS 63244J20 & 63246J20 is LJS.

Related Clinical Trials

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Other records listing Plastimed Laboratoire Pharmaceutique as applicant

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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.