FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SIEMENS SIRECUST 732, PATIENT MONITOR
K Number: K901771
·
Decision May 30, 1990
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
15
Review Days
41
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Basic Information
- Device Name
- SIEMENS SIRECUST 732, PATIENT MONITOR
- K Number
- K901771
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Siemens Medical Electronics
- Date Received
- April 19, 1990
- Decision Date
- May 30, 1990
- Product Code
- DPS
- 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 |
|---|---|---|---|
| DPS | Electrocardiograph | FDA class 2 | Cardiovascular |
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