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

TYPE 4000 TRANSCUTANEOUS ELEC. STIM.

K Number: K800630 · Decision Apr 2, 1980
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
13
Review Days
13

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Basic Information

Device Name
TYPE 4000 TRANSCUTANEOUS ELEC. STIM.
K Number
K800630
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Frye Electronics, Inc.
Date Received
March 20, 1980
Decision Date
April 2, 1980
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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K980377 FONIX FP35 HEARING AID ANALYZER
K935400 FONIX 3500 HEARING AID ANALYZER
K913221 TYPE FA10 AUDIOMETER
K895383 TYPE FP40 DIGITAL HEARING AID ANALYZER
K872242 TYPE 6400 REAL EAR HEARING AID ANALYZER
K861571 TYPE 6500 HEARING AID ANALYZER
K850918 TYPE FP30 DIGITAL HEARING AID ANALYZER
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