FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CLAMP, TUBING, LINE
K Number: K844121
·
Decision Dec 17, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
5
Applicant Total
5
Review Days
55
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Basic Information
- Device Name
- CLAMP, TUBING, LINE
- K Number
- K844121
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 876.4730
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Dyn-A-Med Products
- Date Received
- October 23, 1984
- Decision Date
- December 17, 1984
- Product Code
- FKK
- 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 |
|---|---|---|---|
| FKK | Clamp, Line | FDA class 1 | Gastroenterology, Urology |
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