Exel Secure Touch Safety A.V. Fistula Needle Set

FDA 510(k) K003627 · Exelint International, Co.

Substantially Equivalent

510(k) numberK003627

Submission

Device name
Exel Secure Touch Safety A.V. Fistula Needle Set
Applicant
Exelint International, Co.
Los Angeles, CA, US
Received
November 24, 2000
Decision date
February 8, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FMI – Needle, Hypodermic, Single Lumen
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5570
Specialty
General Hospital

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K251089EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe…FMF · Traditional 12/12/2025SE
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K101309Exelint Aluminum Hub Blunt NeedlesLHI · Traditional 10/20/2010SE
K020189Exel Butterfly Scalp Vein SetFPA · Traditional 03/27/2003SE
K010197Exel Secure Touch Safety (P.S.V.) Scalp Vein SetFPA · Traditional 05/14/2001SE
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Questions and answers

When was Exel Secure Touch Safety A.V. Fistula Needle Set cleared by the FDA?

Exel Secure Touch Safety A.V. Fistula Needle Set (K003627) received a 510(k) decision of Substantially Equivalent on February 8, 2001, 76 days after the submission was received.

What is the product code of K003627?

The FDA product code is FMI – Needle, Hypodermic, Single Lumen, a Class II (moderate risk) device regulated under 21 CFR 880.5570.