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URESIL GASTROSTOMY CATHETER KIT , MODEL GCL-630HBK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093653
510(k) Type
Traditional
Applicant
URESIL, LLC
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/23/2010
Days to Decision
90 days
Submission Type
Statement