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

HEPAX (TENS)

K Number: K882154 · Decision Sep 30, 1988
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
33
Review Days
130

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Basic Information

Device Name
HEPAX (TENS)
K Number
K882154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Avl Scientific Corp.
Date Received
May 23, 1988
Decision Date
September 30, 1988
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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K990092 AVL OMNI MODULAR ANALYZER
K984299 AVL OPTI CRITICAL CARE ANALYZER
K974784 AVL OPTI CRITICAL CARE ANALYZER
K974822 AVL OPTI-CHECK PH/ BLOOD GAS/ ELECTROLYTE/THB/ SO2 CONTROL
K972733 AVL OMNI ANALYZER
K972673 AVL 9181 ELECTROLYTE ANALYZER
K963964 AVL COMPACT 3 PH/BLOOD GAS ANALYZER
Search all 33 clearances from Avl Scientific Corp. →