NS3000 Holmium Laser System— 510(k) K142286
Substantially EquivalentNew Star Lasers, Inc.
FDA 510(k) clearance K142286 for NS3000 Holmium Laser System, Substantially Equivalent on 2014-10-31. Applicant: New Star Lasers, Inc.. Device class: 2.
Clearance details
- Applicant
- New Star Lasers, Inc.
- Product code
- Code GEX
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Roseville, CA, US
Recent devices under product code GEX
view allMore clearances from New Star Lasers, Inc.
view allAdverse 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, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K142286
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K142286.
Data sourced from openFDA. This site is unofficial and independent of the FDA.