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AMPLAID 309 CLINICAL AUDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K880059
510(k) Type
Traditional
Applicant
AMPLUS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1988
Days to Decision
47 days

AMPLAID 309 CLINICAL AUDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K880059
510(k) Type
Traditional
Applicant
AMPLUS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1988
Days to Decision
47 days