NIIC MODEL 15 CARBON-DIOXIDE SURGICAL LASER SYSTEM— 510(k) K902063

Substantially Equivalent

Niic U.S.A., Inc.

FDA 510(k) clearance K902063 for NIIC MODEL 15 CARBON-DIOXIDE SURGICAL LASER SYSTEM, Substantially Equivalent on 1990-06-29. Applicant: Niic U.S.A., Inc..

Clearance details

Applicant: Niic U.S.A., Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1990-05-03
Decision date: 1990-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redwood City, CA, US

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.