FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
iQFlex Pro
K Number: K240009
·
Decision Jul 3, 2024
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
3
Review Days
183
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Basic Information
- Device Name
- iQFlex Pro
- K Number
- K240009
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1720
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- First Source, Inc.
- Date Received
- January 2, 2024
- Decision Date
- July 3, 2024
- 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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