SOF-WICKLAP PAD— 510(k) K780718

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K780718 for SOF-WICKLAP PAD, Substantially Equivalent on 1978-06-28. Applicant: Johnson & Johnson Professionals, Inc..

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code GDY
Advisory panel: General, Plastic Surgery
Date received: 1978-05-01
Decision date: 1978-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Brunswick, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GDY

product code GDY

Malfunction: 764
Total: 764

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.