FDA 510(k)
FDA class 2
Substantially Equivalent
🇧🇷 Brazil
AQUILA 320 D / AQUILA 320 S
K Number: K201340
·
Decision Jun 19, 2020
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
223
Applicant Total
3
Review Days
30
Basic Information
- Device Name
- AQUILA 320 D / AQUILA 320 S
- K Number
- K201340
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 892.1720
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- VMI Tecnologias LTDA
- Date Received
- May 20, 2020
- Decision Date
- June 19, 2020
- 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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