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

INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04

K Number: K933278 · Decision Mar 15, 1995
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
24
Applicant Total
211
Review Days
624

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
K Number
K933278
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intermedics, Inc.
Date Received
June 29, 1993
Decision Date
March 15, 1995
Product Code
KRG
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
KRG Programmer, Pacemaker

Similar 510(k) Clearances

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

View all

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
K922042 CARDIFIX ENDOCARDIAL PACING LEAD
K922972 MODELS 438-05 AND 435-05 IMPLANTABLE 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. →