FDA 510(k) Substantially Equivalent 🇺🇸 United States

STIMULATOR, NERVE, TRANSCUTANEOUS

K Number: K781157 · Decision Sep 20, 1978
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
6
Review Days
77

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Basic Information

Device Name
STIMULATOR, NERVE, TRANSCUTANEOUS
K Number
K781157
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Medtech Intl., Inc.
Date Received
July 5, 1978
Decision Date
September 20, 1978
Advisory Committee
Unknown
Review Advisory Committee
NE
Third Party
N

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