FDA 510(k) Substantially Equivalent 🇺🇸 United States

EGS MODEL 100-2

K Number: K832370 · Decision Sep 16, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
6
Review Days
60

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Basic Information

Device Name
EGS MODEL 100-2
K Number
K832370
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Electro-Med Health Industries, Inc.
Date Received
July 18, 1983
Decision Date
September 16, 1983
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

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