MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM— 510(k) K901340

Substantially Equivalent

Klinger Medical

FDA 510(k) clearance K901340 for MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM, Substantially Equivalent on 1990-06-26. Applicant: Klinger Medical.

Clearance details

Applicant: Klinger Medical
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1990-03-22
Decision date: 1990-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mission Viejo, CA, US

Download summary PDF View on FDA.gov ↗

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.