FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BELZER-MPS
K Number: K972066
·
Decision Nov 26, 1997
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
42
Applicant Total
1
Review Days
176
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Basic Information
- Device Name
- BELZER-MPS
- K Number
- K972066
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5880
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Trans-Med Corp.
- Date Received
- June 3, 1997
- Decision Date
- November 26, 1997
- Product Code
- KDN
- 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 |
|---|---|---|---|
| KDN | System, Perfusion, Kidney | FDA class 2 | Gastroenterology, Urology |
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