Duopro Safety Syringe (Duopross)

FDA 510(k) K020623 · M.K. Meditech Co. , Ltd.

Substantially Equivalent

510(k) numberK020623

Submission

Device name
Duopro Safety Syringe (Duopross)
Applicant
M.K. Meditech Co. , Ltd.
North Attleboro, MA, US
Received
February 26, 2002
Decision date
May 2, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEG – Syringe, Antistick
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Jiangsu Kangbao Medical Equipment Co., Ltd.

510(k)DeviceDecision
K050131Insosafe Bak'Snap Retractable Insulin Safety SyringeMEG · Traditional 04/05/2005SE
K03403110 ML Bak'Snap Duopross Retractable Safety SyringeMEG · Special 01/21/2004SE
K031594Bak'Snap Duopro Safety Syring (Duopross) Safety'Tray Allergy Safety Syringe TrayMEG · Traditional 06/06/2003SE
K022806Duopro Safety Syringe (Duopross)MEG · Special 09/19/2002SE

Questions and answers

When was Duopro Safety Syringe (Duopross) cleared by the FDA?

Duopro Safety Syringe (Duopross) (K020623) received a 510(k) decision of Substantially Equivalent on May 2, 2002, 65 days after the submission was received.

What is the product code of K020623?

The FDA product code is MEG – Syringe, Antistick, a Class II (moderate risk) device regulated under 21 CFR 880.5860.