FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SERVOCARD SCP-840
K Number: K842312
·
Decision Aug 27, 1984
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
5
Review Days
76
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Basic Information
- Device Name
- SERVOCARD SCP-840
- K Number
- K842312
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.5300
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Litton Datamedix
- Date Received
- June 12, 1984
- Decision Date
- August 27, 1984
- Product Code
- LDD
- 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 |
|---|---|---|---|
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) | FDA class 2 | Cardiovascular |
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Other Clearances by Litton Datamedix
| K Number | Device Name | ||
|---|---|---|---|
| K853599 | LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI | Mar 21, 1986 | Substantially Equivalent |
| K850290 | ULTRASOUND GEL | Apr 18, 1985 | Substantially Equivalent |
| K842497 | SERVOMED OXYMONITO SMK 363 | Oct 4, 1984 | Substantially Equivalent |
| K842235 | SERVOCARD DEFIBRILLATOR SCP-851 | Aug 27, 1984 | Substantially Equivalent |