FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VANDERBILT CURETTE
K Number: K761095
·
Decision Nov 30, 1976
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
33
Applicant Total
145
Review Days
8
Basic Information
- Device Name
- VANDERBILT CURETTE
- K Number
- K761095
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 882.4535
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Codman & Shurtleff, Inc.
- Date Received
- November 22, 1976
- Decision Date
- November 30, 1976
- Product Code
- HAO
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HAO | Instrument, Surgical, Non-Powered | FDA class 1 | Neurology |
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