FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DVT SCANNER
K Number: K051980
·
Decision Aug 19, 2005
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
7
Review Days
29
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Basic Information
- Device Name
- DVT SCANNER
- K Number
- K051980
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1750
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Imaging Sciences Intl., Inc.
- Date Received
- July 21, 2005
- Decision Date
- August 19, 2005
- Product Code
- JAK
- 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 |
|---|---|---|---|
| JAK | System, X-Ray, Tomography, Computed | FDA class 2 | Radiology |
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Other Clearances by Imaging Sciences Intl., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K061284 | I-CAT SCANNER | Jul 3, 2006 | Substantially Equivalent |
| K041078 | SURGPLAN AND PANPLAN | Dec 23, 2004 | Substantially Equivalent |
| K001248 | MULTI-PULSE 2000 | May 4, 2000 | Substantially Equivalent |
| K991518 | PANATOME | Jun 18, 1999 | Substantially Equivalent |
| K981466 | XR-910 | Jul 14, 1998 | Substantially Equivalent |
| K931815 | 2000 X-RAY - TOMOGRAPHIC | Aug 23, 1993 | Substantially Equivalent |