FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MICROFLUSH
K Number: K770432
·
Decision Mar 16, 1977
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
48
Review Days
9
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Basic Information
- Device Name
- MICROFLUSH
- K Number
- K770432
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1210
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Medex, Inc.
- Date Received
- March 7, 1977
- Decision Date
- March 16, 1977
- Product Code
- KRA
- 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 |
|---|---|---|---|
| KRA | Catheter, Continuous Flush | FDA class 2 | Cardiovascular |
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| K Number | Device Name | ||
|---|---|---|---|
| K042432 | PHARMGUARD TOOLBOX, MODEL G6000782 | Jan 4, 2005 | Substantially Equivalent |
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| K020780 | TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP | May 20, 2002 | Substantially Equivalent |
| K000328 | MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMP | May 9, 2000 | Substantially Equivalent |
| K982640 | MEDEX 3000 SERIES SYRINGE INFUSION PUMP | Apr 6, 1999 | Substantially Equivalent - Subject to Tracking Reg. |
| K982123 | CONTRAST CONTROL DEVICE | Jul 21, 1998 | Substantially Equivalent |
| K955231 | MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP | Jul 18, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K961404 | MX960 REUSABLE PRESSURE TRANSDUCER | Jun 27, 1996 | Substantially Equivalent |
| K961527 | MX703 AND MX730 CONTINUOUS FLUSH DEVICES | Jun 6, 1996 | Substantially Equivalent |
| K954970 | STOPCOCK & LUER LOCK PLUG | Apr 22, 1996 | Substantially Equivalent |