Biotop Djt-A Safety Syringe

FDA 510(k) K032747 · Biotop Technology Co., Ltd.

Substantially Equivalent

510(k) numberK032747

Submission

Device name
Biotop Djt-A Safety Syringe
Applicant
Biotop Technology Co., Ltd.
Hsin Chu City, TW
Received
September 4, 2003
Decision date
May 11, 2004
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
K062318Biotop Hooksafe U-100 Insulin Syringe, Models 0.5CC/ML and 1CC/MLMEG · Traditional 01/03/2007SE
K043038Biotop Hooksafe Luer-Lock Safety Syringe, Models 3CC/ML, 5CC/ML and 10CC/MLMEG · Special 12/22/2004SE
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Questions and answers

When was Biotop Djt-A Safety Syringe cleared by the FDA?

Biotop Djt-A Safety Syringe (K032747) received a 510(k) decision of Substantially Equivalent on May 11, 2004, 250 days after the submission was received.

What is the product code of K032747?

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