Last synced on 14 November 2025 at 11:06 pm

TENOSNARE

Page Type
Cleared 510(K)
510(k) Number
K970562
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1997
Days to Decision
90 days
Submission Type
Statement

TENOSNARE

Page Type
Cleared 510(K)
510(k) Number
K970562
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1997
Days to Decision
90 days
Submission Type
Statement