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

MODELS 432-03 & 433-03 IMPLANT ENDOCARD PAC LEAD

K Number: K912235 · Decision Sep 18, 1991
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
211
Review Days
127

Basic Information

Device Name
MODELS 432-03 & 433-03 IMPLANT ENDOCARD PAC LEAD
K Number
K912235
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INTERMEDICS, INC.
Date Received
May 14, 1991
Decision Date
September 18, 1991
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 INTERMEDICS, INC.

K Number Device Name
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K962174 BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)
K955550 CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD
K960281 IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY
K954719 INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
K933278 INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
K922042 CARDIFIX ENDOCARDIAL PACING LEAD
K922972 MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD
K920530 INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG
Search all 211 clearances from INTERMEDICS, INC. →