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ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011077
510(k) Type
Special
Applicant
ANDERSEN PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2001
Days to Decision
30 days
Submission Type
Summary