FDA 510(k) FDA class 3 Unknown 🇺🇸 United States

MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD

K Number: K922972 · Decision Jan 22, 1993
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
211
Review Days
217

Basic Information

Device Name
MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD
K Number
K922972
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
INTERMEDICS, INC.
Date Received
June 19, 1992
Decision Date
January 22, 1993
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
K954610 MODEL 430-07 ENDOCARDIAL PACING LEAD
K955122 INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
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
K920530 INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG
K912235 MODELS 432-03 & 433-03 IMPLANT ENDOCARD PAC LEAD
Search all 211 clearances from INTERMEDICS, INC. →