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REAGENTS FOR ORION 1020, AND RELATED ANALYZERS

Page Type
Cleared 510(K)
510(k) Number
K935018
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
90 days
Submission Type
Statement

REAGENTS FOR ORION 1020, AND RELATED ANALYZERS

Page Type
Cleared 510(K)
510(k) Number
K935018
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
90 days
Submission Type
Statement