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DRX5000

Page Type
Cleared 510(K)
510(k) Number
K023160
510(k) Type
Traditional
Applicant
AXIOM USA. INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
88 days
Submission Type
Summary

DRX5000

Page Type
Cleared 510(K)
510(k) Number
K023160
510(k) Type
Traditional
Applicant
AXIOM USA. INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
88 days
Submission Type
Summary