FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VESITEC SUTURE PASSER
K Number: K931181
·
Decision May 12, 1993
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
43
Applicant Total
3
Review Days
64
Basic Information
- Device Name
- VESITEC SUTURE PASSER
- K Number
- K931181
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 876.4730
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- VESITEC MEDICAL, INC.
- Date Received
- March 9, 1993
- Decision Date
- May 12, 1993
- Product Code
- KOA
- 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 |
|---|---|---|---|
| KOA | Surgical Instruments, G-U, Manual (And Accessories) | FDA class 1 | Gastroenterology, Urology |
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