OMNIPULSE HOLMIUM LASER SYSTEM MODEL 1210, OMNIPULSE-MAX HOLMIUM LASER SYSTEM MODELS 1210-VHP, 1500A— 510(k) K992574

Substantially Equivalent

Trimedyne, Inc.

FDA 510(k) clearance K992574 for OMNIPULSE HOLMIUM LASER SYSTEM MODEL 1210, OMNIPULSE-MAX HOLMIUM LASER SYSTEM MODELS 1210-VHP, 1500A, Substantially Equivalent on 1999-10-29. Applicant: Trimedyne, Inc..

Clearance details

Applicant: Trimedyne, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1999-08-02
Decision date: 1999-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, 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.