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REXTON MINI-PRIMO PLUS, PP142, D.C .H.I. FAMILY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953770
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/1995
Days to Decision
35 days
Submission Type
Summary