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AMPLAID A308 CLINICAL AUDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K891988
510(k) Type
Traditional
Applicant
AMPLUS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1989
Days to Decision
198 days

AMPLAID A308 CLINICAL AUDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K891988
510(k) Type
Traditional
Applicant
AMPLUS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1989
Days to Decision
198 days