STAPLE REMOVAL KIT— 510(k) K963234

Substantially Equivalent

Continental Medical Laboratories, Inc.

FDA 510(k) clearance K963234 for STAPLE REMOVAL KIT, Substantially Equivalent on 1996-10-21. Applicant: Continental Medical Laboratories, Inc..

Clearance details

Applicant: Continental Medical Laboratories, Inc.
Product code: Code GDT
Advisory panel: General, Plastic Surgery
Date received: 1996-08-19
Decision date: 1996-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waterford, WI, 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.