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REXTON MODEL 48 AND 49PP

Page Type
Cleared 510(K)
510(k) Number
K970537
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1997
Days to Decision
44 days
Submission Type
Summary

REXTON MODEL 48 AND 49PP

Page Type
Cleared 510(K)
510(k) Number
K970537
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1997
Days to Decision
44 days
Submission Type
Summary