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DIGITAL DIAGNOSTIC ULTRASOUND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K810038
510(k) Type
Traditional
Applicant
ROHE SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1981
Days to Decision
98 days

DIGITAL DIAGNOSTIC ULTRASOUND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K810038
510(k) Type
Traditional
Applicant
ROHE SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1981
Days to Decision
98 days