Last synced on 6 December 2024 at 11:05 pm

FLEX ARM RETRACTOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071338
510(k) Type
Traditional
Applicant
KOROS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2007
Days to Decision
15 days
Submission Type
Statement

FLEX ARM RETRACTOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071338
510(k) Type
Traditional
Applicant
KOROS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2007
Days to Decision
15 days
Submission Type
Statement