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PHACOFRAGMENTATION SYSTEM MEGATRON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002031
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2000
Days to Decision
177 days
Submission Type
Summary

PHACOFRAGMENTATION SYSTEM MEGATRON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002031
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2000
Days to Decision
177 days
Submission Type
Summary