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ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM (INVITRO DIAGNOSTIC SYSTEM WITH 5 ADDITIONAL ASSAYS)

Page Type
Cleared 510(K)
510(k) Number
K993711
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1999
Days to Decision
43 days
Submission Type
Summary

ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM (INVITRO DIAGNOSTIC SYSTEM WITH 5 ADDITIONAL ASSAYS)

Page Type
Cleared 510(K)
510(k) Number
K993711
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1999
Days to Decision
43 days
Submission Type
Summary