FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CONPHAR PERCUSSION HAMMER(BUCK TYPE)
K Number: K803174
·
Decision Dec 30, 1980
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
10
Applicant Total
122
Review Days
15
Basic Information
- Device Name
- CONPHAR PERCUSSION HAMMER(BUCK TYPE)
- K Number
- K803174
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 882.1700
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- CONPHAR, INC.
- Date Received
- December 15, 1980
- Decision Date
- December 30, 1980
- 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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|---|---|---|---|
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| K821276 | MAYO SCISSOR CURYED 5 1/2 | May 28, 1982 | Substantially Equivalent |
| K821273 | MAYO SCISSOR STRAIGHT 6 3/4 | May 28, 1982 | Substantially Equivalent |
| K821285 | SPLINTER FORCEPS 4 1/2 | May 28, 1982 | Substantially Equivalent |
| K821284 | ADSON FORCEPS 4 3/4 | May 28, 1982 | Substantially Equivalent |
| K821292 | TONSIL SCISSORS 7 | May 28, 1982 | Substantially Equivalent |