FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VIRAPUMP II (MODELS AND MODEL M)
K Number: K961607
·
Decision Dec 6, 1996
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
56
Applicant Total
1
Review Days
225
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Basic Information
- Device Name
- VIRAPUMP II (MODELS AND MODEL M)
- K Number
- K961607
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Viatro, Corp.
- Date Received
- April 25, 1996
- Decision Date
- December 6, 1996
- Product Code
- FEB
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FEB | Accessories, Cleaning, For Endoscope | FDA class 2 | Gastroenterology, Urology |
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