FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MAP DC-COUPLED ISOLATED PREAMPLIFIER MODEL #1001
K Number: K885252
·
Decision Jan 13, 1989
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
26
Applicant Total
15
Review Days
30
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Basic Information
- Device Name
- MAP DC-COUPLED ISOLATED PREAMPLIFIER MODEL #1001
- K Number
- K885252
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2060
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Ep Technologies, Inc.
- Date Received
- December 14, 1988
- Decision Date
- January 13, 1989
- Product Code
- DRQ
- 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 |
|---|---|---|---|
| DRQ | Amplifier And Signal Conditioner, Transducer Signal | FDA class 2 | Cardiovascular |
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Other Clearances by Ep Technologies, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K043257 | REAL-TIME POSITION MANAGEMENT (RPM) SYSTEM | Feb 3, 2005 | Substantially Equivalent |
| K013349 | ASTRONOMER PLUS SYSTEM | Apr 9, 2002 | Substantially Equivalent |
| K003452 | POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D | Dec 7, 2000 | Substantially Equivalent |
| K940167 | DIAGNOSTIC I CATHETER | Aug 2, 1994 | Substantially Equivalent |
| K940168 | DIAGNOSTIC II CATHETER | Jul 27, 1994 | Substantially Equivalent |
| K924108 | TRACFINDER II | Dec 16, 1993 | Substantially Equivalent |
| K924109 | STEEROCATH II | Dec 16, 1993 | Substantially Equivalent |
| K913375 | TORQUE TUBE STEEROCATH(TM) | Oct 25, 1991 | Substantially Equivalent |
| K903880 | FRANZ(TM) STEERABLE COMBINATION CATHETER | Oct 12, 1990 | Substantially Equivalent |
| K900765 | STEEROCATH(TM) | May 7, 1990 | Substantially Equivalent |