FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HEMORRHOIDAL LIGATION INSTR. SYSTEM
K Number: K801352
·
Decision Jul 8, 1980
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
21
Applicant Total
303
Review Days
29
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Basic Information
- Device Name
- HEMORRHOIDAL LIGATION INSTR. SYSTEM
- K Number
- K801352
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.4400
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Depuy, Inc.
- Date Received
- June 9, 1980
- Decision Date
- July 8, 1980
- Product Code
- FHN
- 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 |
|---|---|---|---|
| FHN | Ligator, Hemorrhoidal | FDA class 2 | Gastroenterology, Urology |
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