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DIOMED 15, 30, 60 SURGICAL DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K962354
510(k) Type
Traditional
Applicant
LIFESTREAM INT'L, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1996
Days to Decision
85 days
Submission Type
Summary

DIOMED 15, 30, 60 SURGICAL DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K962354
510(k) Type
Traditional
Applicant
LIFESTREAM INT'L, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1996
Days to Decision
85 days
Submission Type
Summary