PRE-PACK TENS— 510(k) K813286

Substantially Equivalent

Cunningham Woodland, Inc.

FDA 510(k) clearance K813286 for PRE-PACK TENS, Substantially Equivalent on 1982-01-22. Applicant: Cunningham Woodland, Inc..

Clearance details

Applicant: Cunningham Woodland, Inc.
Product code: Code GDY
Advisory panel: General, Plastic Surgery
Date received: 1981-11-23
Decision date: 1982-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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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.