FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FRONT-LOAD POLYPROPYLENE SYRINGE
K Number: K001663
·
Decision Nov 16, 2000
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
204
Applicant Total
105
Review Days
169
Basic Information
- Device Name
- FRONT-LOAD POLYPROPYLENE SYRINGE
- K Number
- K001663
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1650
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MEDRAD, INC.
- Date Received
- May 31, 2000
- Decision Date
- November 16, 2000
- Product Code
- DXT
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DXT | Injector And Syringe, Angiographic | FDA class 2 | Cardiovascular |
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| K Number | Device Name | ||
|---|---|---|---|
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| K122916 | JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM JETSTREAM SF 1.6 SYSTEM | Oct 19, 2012 | Substantially Equivalent |
| K113363 | ANGIOJET SOLENT DISTA THROMBECTOMY SET | Jun 6, 2012 | Substantially Equivalent |
| K113133 | MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM), (TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION ARTERION SYRINGE | Dec 15, 2011 | Substantially Equivalent |
| K113428 | ANGIOJET ULTRA DVX THROMBECTOMY SET | Dec 2, 2011 | Substantially Equivalent |
| K112086 | MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM / TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION SYRINGE | Oct 14, 2011 | Substantially Equivalent |
| 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 |