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BETAJECT BD U100

Page Type
Cleared 510(K)
510(k) Number
K833705
510(k) Type
Traditional
Applicant
ORANGE MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1984
Days to Decision
204 days

BETAJECT BD U100

Page Type
Cleared 510(K)
510(k) Number
K833705
510(k) Type
Traditional
Applicant
ORANGE MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1984
Days to Decision
204 days