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ACUSCREEN

Page Type
Cleared 510(K)
510(k) Number
K822782
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1982
Days to Decision
24 days

ACUSCREEN

Page Type
Cleared 510(K)
510(k) Number
K822782
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1982
Days to Decision
24 days