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MODIFIED ENDOGUIDE

Page Type
Cleared 510(K)
510(k) Number
K895559
510(k) Type
Traditional
Applicant
LUXAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1989
Days to Decision
49 days

MODIFIED ENDOGUIDE

Page Type
Cleared 510(K)
510(k) Number
K895559
510(k) Type
Traditional
Applicant
LUXAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1989
Days to Decision
49 days