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ACUPRESS VIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K812902
510(k) Type
Traditional
Applicant
EICONA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1981
Days to Decision
25 days

ACUPRESS VIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K812902
510(k) Type
Traditional
Applicant
EICONA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1981
Days to Decision
25 days