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

STIMULATOR, BATTERY POWERED

K Number: K790123 · Decision Feb 6, 1979
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
211
Review Days
14

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Basic Information

Device Name
STIMULATOR, BATTERY POWERED
K Number
K790123
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Intermedics, Inc.
Date Received
January 23, 1979
Decision Date
February 6, 1979
Product Code
BXN
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BXN Stimulator, Nerve, Battery-Powered

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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
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. →