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ALTADYNE

Page Type
Cleared 510(K)
510(k) Number
K953675
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1995
Days to Decision
52 days
Submission Type
Summary

ALTADYNE

Page Type
Cleared 510(K)
510(k) Number
K953675
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1995
Days to Decision
52 days
Submission Type
Summary