FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
COUDE/ OR TIEMANN
K Number: K103371
·
Decision Mar 11, 2011
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
19
Review Days
114
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Basic Information
- Device Name
- COUDE/ OR TIEMANN
- K Number
- K103371
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5130
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Degania Silicone , Ltd.
- Date Received
- November 17, 2010
- Decision Date
- March 11, 2011
- Product Code
- EZL
- 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 |
|---|---|---|---|
| EZL | Catheter, Retention Type, Balloon | FDA class 2 | Gastroenterology, Urology |
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