FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALPHA NON-INVASIVE BP CARDULE
K Number: K832764
·
Decision Jan 27, 1984
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
46
Review Days
164
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Basic Information
- Device Name
- ALPHA NON-INVASIVE BP CARDULE
- K Number
- K832764
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1130
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Spacelabs, Inc.
- Date Received
- August 16, 1983
- Decision Date
- January 27, 1984
- Product Code
- DXN
- 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 |
|---|---|---|---|
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | FDA class 2 | Cardiovascular |
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|---|---|---|---|
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| K950779 | HEART RATE VARIABILITY SOFTWARE OPTION | Apr 25, 1995 | Substantially Equivalent |
| K941165 | COMET CAPNOGRAPH MODULE | Oct 6, 1994 | Substantially Equivalent |
| K923788 | SPACE LABS MODEL 90560 | Dec 6, 1993 | Substantially Equivalent |
| K912742 | ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE | Apr 20, 1992 | Substantially Equivalent |
| K913038 | SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION | Oct 4, 1991 | Substantially Equivalent |
| K905065 | DEFIBRILLATOR LEAD ADAPTER | Apr 12, 1991 | Substantially Equivalent |
| K910029 | PATIENT CARE MANAGEMENT SYSTEM MODIFICATION | Jan 31, 1991 | Substantially Equivalent |
| K896903 | FIRST MEDIC MODEL 510 | Dec 27, 1990 | Substantially Equivalent |