FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BPROSOFT CASP PC SOFTWARE
K Number: K131916
·
Decision Mar 11, 2014
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
7
Review Days
258
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Basic Information
- Device Name
- BPROSOFT CASP PC SOFTWARE
- K Number
- K131916
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1130
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Healthstats International Pte. , Ltd.
- Date Received
- June 26, 2013
- Decision Date
- March 11, 2014
- 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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| K101002 | A-PULSE CASPRO MODEL T7100, A-PULSE CASPAL MODEL T7200 | Jun 8, 2010 | Substantially Equivalent |
| K072593 | A-PLUS ARTERIAL PULSE WAVEFORM ANALYSIS SYSTEM AND PC SOFTWARE | Nov 15, 2007 | Substantially Equivalent |
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| K051546 | BPCALIBRATOR MC3000/MC3100 | Jun 24, 2005 | Substantially Equivalent |