FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
COMPACT MONITOR SMK 210,211,230,231,240
K Number: K903917
·
Decision Jan 18, 1991
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
161
Applicant Total
3
Review Days
147
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Basic Information
- Device Name
- COMPACT MONITOR SMK 210,211,230,231,240
- K Number
- K903917
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.3535
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Ppg Hellige B.V.
- Date Received
- August 24, 1990
- Decision Date
- January 18, 1991
- Product Code
- DSP
- 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 |
|---|---|---|---|
| DSP | System, Balloon, Intra-Aortic And Control | FDA class 2 | Cardiovascular |
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