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XERAFIT

Page Type
Cleared 510(K)
510(k) Number
K020062
510(k) Type
Traditional
Applicant
METALOR TECHNOLOGIES USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2002
Days to Decision
37 days
Submission Type
Statement

XERAFIT

Page Type
Cleared 510(K)
510(k) Number
K020062
510(k) Type
Traditional
Applicant
METALOR TECHNOLOGIES USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2002
Days to Decision
37 days
Submission Type
Statement