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PROXENON 350, MODEL 902XX

Page Type
Cleared 510(K)
510(k) Number
K071218
510(k) Type
Traditional
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2007
Days to Decision
43 days
Submission Type
Summary

PROXENON 350, MODEL 902XX

Page Type
Cleared 510(K)
510(k) Number
K071218
510(k) Type
Traditional
Applicant
WELCH ALLYN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2007
Days to Decision
43 days
Submission Type
Summary