FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SIRECUST 358
K Number: K803208
·
Decision May 27, 1981
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
66
Review Days
160
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Basic Information
- Device Name
- SIRECUST 358
- K Number
- K803208
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1025
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- December 18, 1980
- Decision Date
- May 27, 1981
- Product Code
- DSI
- 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 |
|---|---|---|---|
| DSI | Detector And Alarm, Arrhythmia | FDA class 2 | Cardiovascular |
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