FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GEMSCOM SERIES 3000

K Number: K914889 · Decision Mar 4, 1992
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
13
Review Days
125

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Basic Information

Device Name
GEMSCOM SERIES 3000
K Number
K914889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
General Devices
Date Received
October 31, 1991
Decision Date
March 4, 1992
Product Code
DRG
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
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

Similar 510(k) Clearances

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Other Clearances by General Devices

K Number Device Name
K013533 EMS TELEMEDICINE OPTION (FOR GEMS SERIES 4000)
K002089 ROSETTA-LT/ROSETTA-RX
K993202 EIM-107 PREP-CHECK
K940009 GEMSCOM SERIES 6000, MODELS 6100, 6200 & 6300
K935839 GEMSCOM SERIES 5000,
K921929 GEMSCOM SERIES 300 12-LEAD ECG (12-LEAD OPTION)
K912008 TRU-VIEW MULTI-CHANNEL DISPLAY
K896153 MODIFIED DR-2C/PMC 100
K862596 DR-2C (MODIFICATION)
K844650 DR-2C
Search all 13 clearances from General Devices →