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ULTRASOUND BREAST SCANNING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K781177
510(k) Type
Traditional
Applicant
LIFE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1979
Days to Decision
181 days

ULTRASOUND BREAST SCANNING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K781177
510(k) Type
Traditional
Applicant
LIFE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1979
Days to Decision
181 days