FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR
K Number: K882160
·
Decision Jun 22, 1988
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
2
Review Days
30
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Basic Information
- Device Name
- COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR
- K Number
- K882160
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Coherent Medical Lasers
- Date Received
- May 23, 1988
- Decision Date
- June 22, 1988
- 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 Coherent Medical Lasers
| K Number | Device Name | ||
|---|---|---|---|
| K884204 | COHERENT EXCELITE CO2 AIR FIBER | Nov 3, 1988 | Substantially Equivalent |