Last synced on 14 November 2025 at 11:06 pm

ADVIA 120 HEMATOLOGY SYSTEM, IN VITRO DIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K971998
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1997
Days to Decision
91 days
Submission Type
Summary

ADVIA 120 HEMATOLOGY SYSTEM, IN VITRO DIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K971998
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1997
Days to Decision
91 days
Submission Type
Summary