Insulin syringe with integrated needle DL

FDA 510(k) K203211 · Dlp Medical Products, Corp.

Substantially Equivalent

510(k) numberK203211

Submission

Device name
Insulin syringe with integrated needle DL
Applicant
Dlp Medical Products, Corp.
San Antonio, TX, US
Received
October 30, 2020
Decision date
February 9, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

Other 510(k)s with product code FMF

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K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)FMF · Traditional Jiangsu Enjosim Medical Technology Co., Ltd.08/14/2026SE
K260208Ultra-Fine™ SAFETY Insulin SyringeFMF · Traditional embecta Medical II, LLC07/13/2026SE
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K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead…FMF · Traditional CMT Health PTE., Ltd.06/12/2026SE
K253112Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special Hlb Lifescience Co., Ltd.05/21/2026SE
K252279Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional Chirana T.Injecta,A.S.04/17/2026SE
K253068Profoject™ Insulin Syringes; Profoject™ Safelock Disposable Insulin SyringeFMF · Traditional CMT Health PTE., Ltd.02/23/2026SE
K253769Instylla Delivery KitFMF · Special Instylla, Inc.12/22/2025SE

Questions and answers

When was Insulin syringe with integrated needle DL cleared by the FDA?

Insulin syringe with integrated needle DL (K203211) received a 510(k) decision of Substantially Equivalent on February 9, 2023, 832 days after the submission was received.

What is the product code of K203211?

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