FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MOBIL-AID AUTOMATIC EXPOSURE CONTROL
K Number: K813128
·
Decision Dec 3, 1981
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
5
Review Days
28
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Basic Information
- Device Name
- MOBIL-AID AUTOMATIC EXPOSURE CONTROL
- K Number
- K813128
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1720
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Advanced Instrument Development, Inc.
- Date Received
- November 5, 1981
- Decision Date
- December 3, 1981
- Product Code
- IZL
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IZL | System, X-Ray, Mobile | FDA class 2 | Radiology |
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Other Clearances by Advanced Instrument Development, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K974863 | IMIX DIGITAL THORAX SYSTEM | Mar 17, 1998 | Substantially Equivalent |
| K872445 | POWER-AID INDEPENDENT X-RAY POWER SOURCE | Aug 12, 1987 | Substantially Equivalent |
| K827525 | AUTOMATIC EXPOSURE CONTROL TYPE A3300 | Jun 18, 1982 | Substantially Equivalent |
| K791933 | CONVERSION CONTRACTOR TIMER KIT | Nov 13, 1979 | Substantially Equivalent |