FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PHILIPS INTEGRIS 3D RA OPTION
K Number: K983877
·
Decision Dec 21, 1998
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
195
Applicant Total
71
Review Days
49
Basic Information
- Device Name
- PHILIPS INTEGRIS 3D RA OPTION
- K Number
- K983877
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1600
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
- Date Received
- November 2, 1998
- Decision Date
- December 21, 1998
- Product Code
- IZI
- 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 |
|---|---|---|---|
| IZI | System, X-Ray, Angiographic | FDA class 2 | Radiology |
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