DIAMOND BLADE SURGICAL KNIVES— 510(k) K895752

Substantially Equivalent

Magnum Diamond, Inc.

FDA 510(k) clearance K895752 for DIAMOND BLADE SURGICAL KNIVES, Substantially Equivalent on 1989-10-17. Applicant: Magnum Diamond, Inc..

Clearance details

Applicant: Magnum Diamond, Inc.
Product code: Code GDM
Advisory panel: General, Plastic Surgery
Date received: 1989-09-26
Decision date: 1989-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rapid City, SD, US

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Adverse events under product code GDM

product code GDM

Death: 2
Total: 2

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.