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FLEXIFLO OVER-THE-GUIDEWIRE GAST KIT W/CR-BAR BUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913786
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
11/5/1991
Days to Decision
74 days
Submission Type
Statement