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AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073034
510(k) Type
Traditional
Applicant
APPLIED MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/14/2008
Days to Decision
140 days
Submission Type
Statement