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PULSTAR

Page Type
Cleared 510(K)
510(k) Number
K992061
510(k) Type
Traditional
Applicant
LASERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
42 days
Submission Type
Statement

PULSTAR

Page Type
Cleared 510(K)
510(k) Number
K992061
510(k) Type
Traditional
Applicant
LASERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
42 days
Submission Type
Statement