FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LOUISVILLE CLAMP PRODUCT #65-172
K Number: K770503
·
Decision Mar 30, 1977
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
140
Review Days
14
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Basic Information
- Device Name
- LOUISVILLE CLAMP PRODUCT #65-172
- K Number
- K770503
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4450
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Edward Weck, Inc.
- Date Received
- March 16, 1977
- Decision Date
- March 30, 1977
- Product Code
- DXC
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DXC | Clamp, Vascular | FDA class 2 | Cardiovascular |
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