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DILATOR TUBE SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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