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

3038 OPTION B-COMPUT. TRANS. TERMINAL

K Number: K761318 · Decision Jan 6, 1977
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
292
Applicant Total
13
Review Days
10

Basic Information

Device Name
3038 OPTION B-COMPUT. TRANS. TERMINAL
K Number
K761318
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
CAMBRIDGE INSTRUMENTS, INC.
Date Received
December 27, 1976
Decision Date
January 6, 1977
Product Code
DXH
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
DXH Transmitters And Receivers, Electrocardiograph, Telephone

Similar 510(k) Clearances

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

View all

Other Clearances by CAMBRIDGE INSTRUMENTS, INC.

K Number Device Name
K811121 CENTRAL STATION MONITORING SYSTEMS
K811062 CAMPBRIDGE COMPUTRACE
K803229 4-CHANNEL ECG TELEMETRY MON. SYST. #3045
K801224 CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEM
K800566 CAMBRIDGE VS-550 ELECTROCARDIOGRAPH
K792661 TREADMILL MODEL 3060
K791201 SCINTISTRESS SYSTEM
K790509 CARDIOCASSETTE II, AMBULATORY ECG SYSTEM
K761198 MODEL 3044 3-CHANNEL STRESS TEST SYSTEM
K760926 ELECTROCARDIOGRAPH (MODEL VS-4B)
Search all 13 clearances from CAMBRIDGE INSTRUMENTS, INC. →