FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SKIN ADHESIVE-50XX
K Number: K812249
·
Decision Sep 23, 1981
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
4
Review Days
43
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Basic Information
- Device Name
- SKIN ADHESIVE-50XX
- K Number
- K812249
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5250
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Manfred Sauer Corp.
- Date Received
- August 11, 1981
- Decision Date
- September 23, 1981
- 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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