FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LASER SYSTEM YELLOWSTAR
K Number: K013940
·
Decision Feb 26, 2002
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
5
Review Days
89
Basic Information
- Device Name
- LASER SYSTEM YELLOWSTAR
- K Number
- K013940
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ASCLEPION-MEDITEC AG
- Date Received
- November 29, 2001
- Decision Date
- February 26, 2002
- Product Code
- GEX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | FDA class 2 | General, Plastic Surgery |
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Other Clearances by ASCLEPION-MEDITEC AG
| K Number | Device Name | ||
|---|---|---|---|
| K021975 | LASERSYSTEM BEAUTYSTAR 532 | Sep 13, 2002 | Substantially Equivalent |
| K014057 | DERMASTAR ER:YAG LASER SYSTEM | Mar 8, 2002 | Substantially Equivalent |
| K002031 | PHACOFRAGMENTATION SYSTEM MEGATRON | Dec 27, 2000 | Substantially Equivalent |
| K002032 | C02 LASER MULTIPULSE | Sep 11, 2000 | Substantially Equivalent |