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OMNIPROBE ELECTRICAL NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K831147
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
101 days

OMNIPROBE ELECTRICAL NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K831147
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
101 days