FDA 510(k) clearance · back to tracker

Pro-Line XL Power Injectable Central Venous Catheter and Pro-Line XL Tunneler

Medical Components, Inc. cleared K260080 on 2026-10-09, decision: substantially equivalent

K-number

K260080

Sponsor

Medical Components, Inc.

Device

Pro-Line XL Power Injectable Central Venous Catheter and Pro-Line XL Tunneler

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-10-09

Product code

LJS

Advisory committee

General Hospital

Medical specialty

General Hospital

Regulation number

880.5970

Official FDA record

Open K260080on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K260080 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.