FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CONPHAR PERCUSSION HAMMER(TAYLOR)
K Number: K803148
·
Decision Jan 8, 1981
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
10
Applicant Total
122
Review Days
27
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Basic Information
- Device Name
- CONPHAR PERCUSSION HAMMER(TAYLOR)
- K Number
- K803148
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 882.1700
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Conphar, Inc.
- Date Received
- December 12, 1980
- Decision Date
- January 8, 1981
- Product Code
- GWZ
- 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 |
|---|---|---|---|
| GWZ | Percussor | FDA class 1 | Neurology |
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| K821275 | MAYO SCISSOR STRAIGHT 5 1/2 | May 28, 1982 | Substantially Equivalent |
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