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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LDD), ordered by most recent decision date.

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Other Clearances by Litton Datamedix

K Number Device Name
K853599 LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI
K850290 ULTRASOUND GEL
K842497 SERVOMED OXYMONITO SMK 363
K842235 SERVOCARD DEFIBRILLATOR SCP-851