FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
P3T ABDOMEN
K Number: K082458
·
Decision Oct 17, 2008
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
105
Review Days
52
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Basic Information
- Device Name
- P3T ABDOMEN
- K Number
- K082458
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1750
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medrad, Inc.
- Date Received
- August 26, 2008
- Decision Date
- October 17, 2008
- Product Code
- JAK
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- Y
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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| K113133 | MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM), (TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION ARTERION SYRINGE | Dec 15, 2011 | Substantially Equivalent |
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| K111182 | ANGIOJET SOLENT OMNI THROMBECTOMY SET | May 24, 2011 | Substantially Equivalent |
| K100798 | MEDRAD INTEGO PET INFUSION SYSTEM, SOURCE ADMINISTRATION SET, PATIENT ADMINSTRATIN SET MODEL INT SYS 100, INT CSS, INT C | Jun 23, 2010 | Substantially Equivalent |