K952008

Substantially Equivalent

KARL STORZ DRILL

Applicant: KARL STORZ Endoscopy-America, Inc.
Product code: GEY
Advisory panel: General, Plastic Surgery
Date received: 1995-04-28
Decision date: 1995-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Adverse events under product code GEY

product code GEY

Malfunction: 7,488
Total: 7,488

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.