FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
URO PRO
K Number: K042457
·
Decision Oct 25, 2004
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
27
Applicant Total
15
Review Days
45
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Basic Information
- Device Name
- URO PRO
- K Number
- K042457
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5130
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- W.O.M. World of Medicine AG
- Date Received
- September 10, 2004
- Decision Date
- October 25, 2004
- Product Code
- LJH
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| LJH | System, Irrigation, Urological | FDA class 2 | Gastroenterology, Urology |
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