CATHTONG II PICC Catheter
K-Number: K172039 · 2017-08-03
ApplicantL&Z Us, Inc.
Decision Date2017-08-03
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
CATHTONG II PICC Catheter is a medical device manufactured by L&Z Us, Inc.. It received FDA 510(k) clearance on 2017-08-03 under approval number K172039. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CATHTONG II PICC Catheter?
CATHTONG II PICC Catheter is a medical device that received FDA 510(k) clearance on 2017-08-03. It is manufactured by L&Z Us, Inc.. The 510(k) number is K172039.
When was CATHTONG II PICC Catheter approved by the FDA?
CATHTONG II PICC Catheter received FDA 510(k) clearance on 2017-08-03, under approval number K172039.
What company makes CATHTONG II PICC Catheter?
CATHTONG II PICC Catheter is manufactured by L&Z Us, Inc..
What is the FDA product code for CATHTONG II PICC Catheter?
The FDA product code for CATHTONG II PICC Catheter is LJS.
Other Devices by L&Z Us, Inc.
Related Devices (Code: LJS)
K160925VPS Rhythm Device with TipTracker TechnologyArrow International, Inc. (A Subsidiary of Teleflex, Inc.)
K162443PowerPICC Provena CathetersC.R. Bard, Inc.
K161496Turbo-Flo PICC SetsCook Incorporated
K161765CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex
K153469Cathtong I PICC CatheterL&Z Us, Inc.
K151985PowerPICC® EtOH Catheter and PowerPICC SOLO®2 EtOH CatheterC.R. Bard, Inc.
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.