FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFIED FLOCATH PULMONARY ARTERY CATHETER
K Number: K901733
·
Decision Jul 16, 1990
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
136
Applicant Total
23
Review Days
90
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MODIFIED FLOCATH PULMONARY ARTERY CATHETER
- K Number
- K901733
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2100
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Cardio Metrics, Inc.
- Date Received
- April 17, 1990
- Decision Date
- July 16, 1990
- Product Code
- DPW
- 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 |
|---|---|---|---|
| DPW | Flowmeter, Blood, Cardiovascular | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DPW), ordered by most recent decision date.
FloPatch FP120
FDA 510(k)
FDA Class 2
·Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)
FDA 510(k)
FDA Class 2
·Cardiovascular
FloPatch FP120
FDA 510(k)
FDA Class 2
·Cardiovascular
Elfor-L
FDA 510(k)
FDA Class 2
·Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)
FDA 510(k)
FDA Class 2
·Cardiovascular
FloPatch FP120
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by Cardio Metrics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K972762 | CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES | Oct 14, 1997 | Substantially Equivalent |
| K965140 | CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEM | Aug 18, 1997 | Substantially Equivalent |
| K951567 | CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE | Oct 25, 1996 | Substantially Equivalent |
| K961777 | ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404 | Jul 31, 1996 | Substantially Equivalent |
| K955551 | CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 | Feb 28, 1996 | Substantially Equivalent |
| K954913 | CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION) | Nov 7, 1995 | Substantially Equivalent |
| K952562 | CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE | Aug 29, 1995 | Substantially Equivalent |
| K943022 | CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE | Sep 19, 1994 | Substantially Equivalent |
| K940984 | CARDIOMETRICS DUALFLOW SWITCH BOX | Aug 18, 1994 | Substantially Equivalent |
| K933320 | CARDIOMETRICS FLOMAP AND FLOMOD ULTRASOUND INSTRUMENT | Aug 17, 1994 | Substantially Equivalent |