FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
URIFIX
K Number: K813537
·
Decision Jan 12, 1982
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
3
Review Days
25
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Basic Information
- Device Name
- URIFIX
- K Number
- K813537
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5250
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Isramed, Inc.
- Date Received
- December 18, 1981
- Decision Date
- January 12, 1982
- 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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