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MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted 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