LIHTAN 532 LASER— 510(k) K951117

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K951117 for LIHTAN 532 LASER, Substantially Equivalent on 1995-10-18. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 1995-03-10
Decision date: 1995-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, 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.