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MODIFIED LIFECARE MODEL 175 INFUSER

Page Type
Cleared 510(K)
510(k) Number
K912092
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1991
Days to Decision
81 days
Submission Type
Statement

MODIFIED LIFECARE MODEL 175 INFUSER

Page Type
Cleared 510(K)
510(k) Number
K912092
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1991
Days to Decision
81 days
Submission Type
Statement