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MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K990863
510(k) Type
Special
Applicant
ROSS PRODUCT DIV. ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1999
Days to Decision
21 days
Submission Type
Statement

MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K990863
510(k) Type
Special
Applicant
ROSS PRODUCT DIV. ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1999
Days to Decision
21 days
Submission Type
Statement