FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SOPRO 162 CAMERA
K Number: K070102
·
Decision Feb 20, 2007
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
25
Review Days
41
Basic Information
- Device Name
- SOPRO 162 CAMERA
- K Number
- K070102
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SOPRO
- Date Received
- January 10, 2007
- Decision Date
- February 20, 2007
- Product Code
- GCJ
- Advisory Committee
- Gastroenterology, Urology
- 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 |
|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | FDA class 2 | Gastroenterology, Urology |
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| K072912 | SOPRO 225 DUAL HALOGEN LIGHT SOURCE | Nov 16, 2007 | Substantially Equivalent |
| K031593 | SOPRO 61D | Sep 16, 2003 | Substantially Equivalent |