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FLEXIFLO OVER-THE-GUIDEWIRE GASTROSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915110
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
4/14/1992
Days to Decision
153 days
Submission Type
Statement