FDA 510(k)

L-CATH CATHETER SYSTEM - PORT L-CATH

K-Number: K942103 · 1994-07-26

Decision Date1994-07-26

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

L-CATH CATHETER SYSTEM - PORT L-CATH is the device name listed in this FDA 510(k) record. The listed applicant is Luther Medical Products, Inc.. It received FDA 510(k) clearance on 1994-07-26 under 510(k) number K942103. 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 L-CATH CATHETER SYSTEM - PORT L-CATH?

L-CATH CATHETER SYSTEM - PORT L-CATH is a medical device that received FDA 510(k) clearance on 1994-07-26. The listed applicant is Luther Medical Products, Inc.. The 510(k) number is K942103.

When did L-CATH CATHETER SYSTEM - PORT L-CATH receive FDA 510(k) clearance?

L-CATH CATHETER SYSTEM - PORT L-CATH received FDA 510(k) clearance on 1994-07-26, under 510(k) number K942103.

Who is the listed applicant for L-CATH CATHETER SYSTEM - PORT L-CATH?

The FDA 510(k) record lists Luther Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-CATH CATHETER SYSTEM - PORT L-CATH?

The FDA product code for L-CATH CATHETER SYSTEM - PORT L-CATH is LJT.

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Other records listing Luther Medical Products, Inc. as applicant

K982797BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB K980090ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)K974543L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGER K940198L-CATH CONNECTOR ASSEMBLY K930473ONECATH L-CATH CATHETER SYSTEM K925236L CATH(R) CATHETER SYSTEM

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Related Devices (Code: LJT)

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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.