FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AIR UTERINE DISPLACER-AUD 120
K Number: K833022
·
Decision Oct 14, 1983
Classifications
1
FEI Numbers
279
Registration Numbers
280
Same Product Code
7
Applicant Total
11
Review Days
38
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Basic Information
- Device Name
- AIR UTERINE DISPLACER-AUD 120
- K Number
- K833022
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.6820
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Scientific Sales Intl., Inc.
- Date Received
- September 6, 1983
- Decision Date
- October 14, 1983
- Product Code
- CCX
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CCX | Support, Patient Position | FDA class 1 | Anesthesiology |
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