FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PINNACLE 3
K Number: K926008
·
Decision Oct 4, 1994
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
88
Review Days
676
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Basic Information
- Device Name
- PINNACLE 3
- K Number
- K926008
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Adac Laboratories
- Date Received
- November 27, 1992
- Decision Date
- October 4, 1994
- Product Code
- IYE
- 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 |
|---|---|---|---|
| IYE | Accelerator, Linear, Medical | FDA class 2 | Radiology |
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| K041218 | GRIFFIN SPECT/CT IMAGING SYSTEM | May 24, 2004 | Substantially Equivalent |
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