SDR 3500 (PHILIPS PLATINUM +)— 510(k) K873937

Name: FDA 510(k) clearance K873937
Creator: U.S. Food and Drug Administration
Published: 1988-03-23

Substantially Equivalent

Philips Ultrasound, Inc.

FDA 510(k) clearance K873937 for SDR 3500 (PHILIPS PLATINUM +), Substantially Equivalent on 1988-03-23. Applicant: Philips Ultrasound, Inc.. Device class: 2.

Clearance details

Applicant: Philips Ultrasound, Inc.
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1987-09-28
Decision date: 1988-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.