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LASERTX - DIODE LASER & DELIVERY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060326
510(k) Type
Traditional
Applicant
Prosurg, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2006
Days to Decision
55 days
Submission Type
Statement

LASERTX - DIODE LASER & DELIVERY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060326
510(k) Type
Traditional
Applicant
Prosurg, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2006
Days to Decision
55 days
Submission Type
Statement