SKIN STAPLE REMOVER KIT— 510(k) K915430

Unknown

Cypress Medical Products, Ltd.

FDA 510(k) clearance K915430 for SKIN STAPLE REMOVER KIT, Unknown on 1992-02-28. Applicant: Cypress Medical Products, Ltd..

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code GDT
Advisory panel: General, Plastic Surgery
Date received: 1991-12-02
Decision date: 1992-02-28
Decision: Unknown
Clearance type: Traditional
Location: Mc Henry, IL, US

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Adverse events under product code GDT

product code GDT

Malfunction: 752
Total: 752

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.