FDA 510(k) clearance · back to tracker

ACUNAV Luxera 4D ICE Catheter

Siemens Medical Solutions USA, Inc. cleared K261696 on 2026-09-10, decision: substantially equivalent

K-number

K261696

Sponsor

Siemens Medical Solutions USA, Inc.

Device

ACUNAV Luxera 4D ICE Catheter

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-09-10

Product code

OBJ

Advisory committee

Cardiovascular

Medical specialty

Cardiovascular

Regulation number

870.1200

Official FDA record

Open K261696on 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 K261696 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.

Try the sandbox

Source

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