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FLEXIFLO LAPAROSCOPIC JEJUNOSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K925102
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/9/1994
Days to Decision
609 days
Submission Type
Statement

FLEXIFLO LAPAROSCOPIC JEJUNOSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K925102
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/9/1994
Days to Decision
609 days
Submission Type
Statement