FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RAPSODY(TM) REAL-TIME ARRHYTHMIA PROCESSING SYSTEM
K Number: K911835
·
Decision Feb 14, 1992
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
1
Review Days
295
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Basic Information
- Device Name
- RAPSODY(TM) REAL-TIME ARRHYTHMIA PROCESSING SYSTEM
- K Number
- K911835
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1025
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Gs Microsystems
- Date Received
- April 25, 1991
- Decision Date
- February 14, 1992
- 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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