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GENESIS II TRANSCRANIAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K883238
510(k) Type
Traditional
Applicant
BIOSOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1988
Days to Decision
23 days

GENESIS II TRANSCRANIAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K883238
510(k) Type
Traditional
Applicant
BIOSOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1988
Days to Decision
23 days