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

NEUROMEDICS ORIONS #660-01

K Number: K822600 · Decision Sep 24, 1982
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
211
Review Days
28

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Basic Information

Device Name
NEUROMEDICS ORIONS #660-01
K Number
K822600
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Intermedics, Inc.
Date Received
August 27, 1982
Decision Date
September 24, 1982
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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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. →