FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARGON LASER SYS-MODEL 5000
K Number: K832703
·
Decision Jan 30, 1984
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
5
Review Days
172
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Basic Information
- Device Name
- ARGON LASER SYS-MODEL 5000
- K Number
- K832703
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Cooper Medical Corp.
- Date Received
- August 11, 1983
- Decision Date
- January 30, 1984
- Product Code
- HQE
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HQE | Instrument, Vitreous Aspiration And Cutting, Ac-Powered | FDA class 2 | Ophthalmic |
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Other Clearances by Cooper Medical Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K840144 | YAG LASER 8000 GASTROINTESTINAL BLEE | May 18, 1984 | Substantially Equivalent |
| K833387 | ARGON LASER SURGICAL SYSTEM 770 | Apr 18, 1984 | Substantially Equivalent |
| K833497 | COOPER MEDICAL MODEL 770 | Apr 17, 1984 | Substantially Equivalent |
| K820261 | MONITOR CO2 LASER SYSTEM | Mar 5, 1982 | Substantially Equivalent |