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WEBERNEEDLE BASIC LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073352
510(k) Type
Traditional
Applicant
Weber Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/11/2008
Days to Decision
256 days
Submission Type
Summary

WEBERNEEDLE BASIC LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073352
510(k) Type
Traditional
Applicant
Weber Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/11/2008
Days to Decision
256 days
Submission Type
Summary