ENDOPATH XCEL BLADELESS TROCAR WITH OPTIVIEW TECHNOLOGY ENDOPATH XCEL BLUNT TIP TROCAR WITH OPTIVIEW TECHNOLOGY ENDOPATH

FDA 510(k) Premarket Notification · Submission K122511 · Applicant: Ethicon Endo-Surgery, LLC

Public Record 510(k) Submission Decision Date: 2012-10-01 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K122511.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K122511
Applicant / Sponsor
Device Name
ENDOPATH XCEL BLADELESS TROCAR WITH OPTIVIEW TECHNOLOGY ENDOPATH XCEL BLUNT TIP TROCAR WITH OPTIVIEW TECHNOLOGY ENDOPATH
Product Code
GCJ
Decision Date
2012-10-01
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Gastroenterology, Urology (GU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2012-08-17

Related Establishments / Registrations

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