FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.

K Number: K760714 · Decision Dec 14, 1976
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
15
Review Days
80

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Basic Information

Device Name
ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.
K Number
K760714
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Coratomic, Inc.
Date Received
September 25, 1976
Decision Date
December 14, 1976
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

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Other Clearances by Coratomic, Inc.

K Number Device Name
K863365 MODIFICATION OF STERILITY CYCLE PARAMETERS
K822791 CORATOMIC #VX5-105 & VX5-205 PULSE GEN.
K820939 C-101-P
K821014 CORATOMIC MODEL OVALITH 920BP
K821033 CORATOMIC MODEL OVALITH-920
K810808 CORATOMIC MODEL OVALITH-920
K802689 L-15T ENDOCARDIAL PACING ELECTRODE
K800194 OVALITH P-BP BIPOLAR CARDIAC PACEMAKER
K790446 OVALITH-300
K781377 OVALITH 10BP
Search all 15 clearances from Coratomic, Inc. →