FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIBAG
K Number: K791198
·
Decision Jul 30, 1979
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
3
Review Days
34
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Basic Information
- Device Name
- BIBAG
- K Number
- K791198
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5250
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Ab Medett Produkter
- Date Received
- June 26, 1979
- Decision Date
- July 30, 1979
- Product Code
- KNX
- 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 |
|---|---|---|---|
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | FDA class 2 | Gastroenterology, Urology |
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