FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FUJI EC ID CAMERA
K Number: K932357
·
Decision Jul 26, 1993
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
17
Applicant Total
71
Review Days
73
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Basic Information
- Device Name
- FUJI EC ID CAMERA
- K Number
- K932357
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1640
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Date Received
- May 14, 1993
- Decision Date
- July 26, 1993
- Product Code
- JAC
- 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 |
|---|---|---|---|
| JAC | System, X-Ray, Film Marking, Radiographic | FDA class 1 | Radiology |
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