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REXPLUS PP3

Page Type
Cleared 510(K)
510(k) Number
K944548
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
59 days
Submission Type
Summary

REXPLUS PP3

Page Type
Cleared 510(K)
510(k) Number
K944548
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
59 days
Submission Type
Summary