FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IMALUX OCT IMAGING SYSTEM
K Number: K033783
·
Decision Mar 1, 2004
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
45
Applicant Total
1
Review Days
88
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Basic Information
- Device Name
- IMALUX OCT IMAGING SYSTEM
- K Number
- K033783
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Imalux Coporation
- Date Received
- December 4, 2003
- Decision Date
- March 1, 2004
- Product Code
- NQQ
- Advisory Committee
- Radiology
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| NQQ | System, Imaging, Optical Coherence Tomography (Oct) | FDA class 2 | Radiology |
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