Biotop Hooksafe Luer-Lock Safety Syringe, Models 3CC/ML, 5CC/ML and 10CC/ML

FDA 510(k) K043038 · Biotop Technology Co., Ltd.

Substantially Equivalent

510(k) numberK043038

Submission

Device name
Biotop Hooksafe Luer-Lock Safety Syringe, Models 3CC/ML, 5CC/ML and 10CC/ML
Applicant
Biotop Technology Co., Ltd.
Taipei, TW
Received
November 4, 2004
Decision date
December 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
K062318Biotop Hooksafe U-100 Insulin Syringe, Models 0.5CC/ML and 1CC/MLMEG · Traditional 01/03/2007SE
K041970Biotop Hooksafe Safety Syringe, Models 0.5CC/ML, 1CC/ML, 3CC/ML, 5CC/ML and 10CC/MLMEG · Special 08/03/2004SE
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Questions and answers

When was Biotop Hooksafe Luer-Lock Safety Syringe, Models 3CC/ML, 5CC/ML and 10CC/ML cleared by the FDA?

Biotop Hooksafe Luer-Lock Safety Syringe, Models 3CC/ML, 5CC/ML and 10CC/ML (K043038) received a 510(k) decision of Substantially Equivalent on December 22, 2004, 48 days after the submission was received.

What is the product code of K043038?

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