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BETA SCAN NORMAL CONTROL SOLUTION

Page Type
Cleared 510(K)
510(k) Number
K831523
510(k) Type
Traditional
Applicant
ORANGE MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1983
Days to Decision
68 days

BETA SCAN NORMAL CONTROL SOLUTION

Page Type
Cleared 510(K)
510(k) Number
K831523
510(k) Type
Traditional
Applicant
ORANGE MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1983
Days to Decision
68 days