K854743

Substantially Equivalent

2.5 MHZ PHASED ARRAY SECTOR MERIDIAN PROBE

Applicant: Johnson & Johnson Professionals, Inc.
Product code: IYO
Advisory panel: Radiology
Date received: 1985-11-25
Decision date: 1986-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ramsey, NJ, US

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.