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REVEEL ENDOSCOPIC RETRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133345
510(k) Type
Traditional
Applicant
RETRACTION LIMITED
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/11/2014
Days to Decision
163 days
Submission Type
Summary