TMD 0.5ML Safety Syringe (FA18 Series 0.5ML/FA58 Series U-100 INSULIN/FA78 Series Tuberculin)

FDA 510(k) K042426 · Taiject Medical Device Co., Ltd.

Substantially Equivalent

510(k) numberK042426

Submission

Device name
TMD 0.5ML Safety Syringe (FA18 Series 0.5ML/FA58 Series U-100 INSULIN/FA78 Series Tuberculin)
Applicant
Taiject Medical Device Co., Ltd.
Newport Beach, CA, US
Received
September 8, 2004
Decision date
September 22, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 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
K031062TMD 1ML Safety Syringe (FA11 Series 1ML/FA51 Series U-100 INSULIN/FA71 Series Tuberculin)MEG · Special 05/02/2003SE
K023458TMD Safety Syringe (FA14 Series 10ML/FA15 Series 20ML)MEG · Special 11/07/2002SE
K022278TMD Safety Syringe (FA12 Series 3ML/FA13 Series 5ML)MEG · Traditional 09/12/2002SE

Questions and answers

When was TMD 0.5ML Safety Syringe (FA18 Series 0.5ML/FA58 Series U-100 INSULIN/FA78 Series Tuberculin) cleared by the FDA?

TMD 0.5ML Safety Syringe (FA18 Series 0.5ML/FA58 Series U-100 INSULIN/FA78 Series Tuberculin) (K042426) received a 510(k) decision of Substantially Equivalent on September 22, 2004, 14 days after the submission was received.

What is the product code of K042426?

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