FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SNARE
K Number: K960230
·
Decision Jul 31, 1996
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
61
Applicant Total
4
Review Days
196
Basic Information
- Device Name
- SNARE
- K Number
- K960230
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.4300
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- LIGHTHOUSE MEDICAL, INC.
- Date Received
- January 17, 1996
- Decision Date
- July 31, 1996
- Product Code
- FDI
- 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 |
|---|---|---|---|
| FDI | Snare, Flexible | FDA class 2 | Gastroenterology, Urology |
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