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LUXSCOPE

Page Type
Cleared 510(K)
510(k) Number
K973193
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1997
Days to Decision
88 days
Submission Type
Statement

LUXSCOPE

Page Type
Cleared 510(K)
510(k) Number
K973193
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1997
Days to Decision
88 days
Submission Type
Statement