FDA 510(k)

RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD

K-Number: K122781 · 2013-02-05

ApplicantCovidien, Formerly US Surgical A Divison of Tyco H

Decision Date2013-02-05

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, Formerly US Surgical A Divison of Tyco H. It received FDA 510(k) clearance on 2013-02-05 under 510(k) number K122781. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD?

RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD is a medical device that received FDA 510(k) clearance on 2013-02-05. The listed applicant is Covidien, Formerly US Surgical A Divison of Tyco H. The 510(k) number is K122781.

When did RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD receive FDA 510(k) clearance?

RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD received FDA 510(k) clearance on 2013-02-05, under 510(k) number K122781.

Who is the listed applicant for RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD?

The FDA 510(k) record lists Covidien, Formerly US Surgical A Divison of Tyco H as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD?

The FDA product code for RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD is GDW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Covidien, Formerly US Surgical A Divison of Tyco H as applicant

K131705ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY K130532IDRIVE ULTRA STERILIZATION TRAY K130717ENDO GIA RELOAD K130435VERSAPORT V2 BLADELESS OPTICAL TROCAR K123318IDRIVE ULTRA POWERED HANDLE AND ENDO GIA ADAPTER K121510IDRIVE ULTRA POWERED HANDLE ENDO GIA ADAPTER

View all 13 devices →

Related Devices (Code: GDW)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.