FDA 510(k) clearance · back to tracker

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System

Philips Ultrasound, LLC cleared K233788 on 2024-02-13, decision: substantially equivalent

K-number

K233788

Sponsor

Philips Ultrasound, LLC

Device

EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System

Class

Class II

Decision

Substantially Equivalent

Decision date

2024-02-13

Product code

IYN

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1550

Official FDA record

Open K233788on 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.

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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.