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COMPAT JEJUNOSTOMY TUBE KIT, MODEL 088OXX (XX=16,14, OR 12)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991668
510(k) Type
Traditional
Applicant
NOVARTIS NUTRITION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1999
Days to Decision
73 days
Submission Type
Summary