FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY
K Number: K082876
·
Decision Nov 10, 2008
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
4
Review Days
42
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Basic Information
- Device Name
- BEAMAX/ FORMAX PULSED LIGHT DEVICE FAMILY
- K Number
- K082876
- 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
- Sharplight Technologies, Ltd.
- Date Received
- September 29, 2008
- Decision Date
- November 10, 2008
- 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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