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LAPAROSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973891
510(k) Type
Traditional
Applicant
APPLIED MEDICAL RESOURCES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1998
Days to Decision
90 days
Submission Type
Summary