FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EFFRON PAROTID RETRACTOR
K Number: K801759
·
Decision Aug 20, 1980
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
99
Applicant Total
31
Review Days
23
Basic Information
- Device Name
- EFFRON PAROTID RETRACTOR
- K Number
- K801759
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- AMERICAN V. MUELLER
- Date Received
- July 28, 1980
- Decision Date
- August 20, 1980
- Product Code
- GAD
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GAD | Retractor | FDA class 1 | General, Plastic Surgery |
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