Last synced on 25 January 2026 at 3:41 am

MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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