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C02 LASER MULTIPULSE

Page Type
Cleared 510(K)
510(k) Number
K002032
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2000
Days to Decision
70 days
Submission Type
Summary

C02 LASER MULTIPULSE

Page Type
Cleared 510(K)
510(k) Number
K002032
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2000
Days to Decision
70 days
Submission Type
Summary