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

NEUROMEDICS ULTRASTIM 650-01

K Number: K841647 · Decision Jul 3, 1984
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
211
Review Days
74

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Basic Information

Device Name
NEUROMEDICS ULTRASTIM 650-01
K Number
K841647
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Intermedics, Inc.
Date Received
April 20, 1984
Decision Date
July 3, 1984
Product Code
IPF
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IPF Stimulator, Muscle, 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. →