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DILATOR TUBE SET

Page Type
Cleared 510(K)
510(k) Number
K120590
510(k) Type
Traditional
Applicant
KOROS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2013
Days to Decision
434 days
Submission Type
Statement

DILATOR TUBE SET

Page Type
Cleared 510(K)
510(k) Number
K120590
510(k) Type
Traditional
Applicant
KOROS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2013
Days to Decision
434 days
Submission Type
Statement