SOL-GUARD Safety Pull Button Collection Set

FDA 510(k) K213718 · Sol-Millennium Medical, Inc.

Substantially Equivalent

510(k) numberK213718

Submission

Device name
SOL-GUARD Safety Pull Button Collection Set
Applicant
Sol-Millennium Medical, Inc.
Suwanee, GA, US
Received
November 24, 2021
Decision date
August 30, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1675
Specialty
Clinical Chemistry

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More from Sol-Millennium Medical, Inc.

510(k)DeviceDecision
K252184SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional 08/25/2026SE
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K250907Sol-Guard TM XtraThin Safety Pull-Button Blood Collection SetJKA · Special 04/30/2025SE
K242291SOL-M Luer Lock Syringe (Low Dead Space) w/o Needle, SOL-M Slip Tip Syringe (Low Dead…QNQ · Traditional 11/20/2024SE
K242099Sol-M™ Slip Tip Syringe without Needle, Sol-M™ Eccentric Tip Syringe without NeedleFMF · Traditional 10/22/2024SE
K241821Luer Lock Syringe with Safety Needle; Luer Lock Syringe with Exchangeable Needle; Luer…FMF · Traditional 09/20/2024SE
K220713Sol-Guard Auto-disable SyringeFMF · Traditional 05/04/2023SE
K222744Sol-M Luer Lock SyringeFMF · Special 10/11/2022SE
K182146Sol-M Blood Collection Needles, Sol-Care Safety Blood Collection Needles, Sol-Care…FMI · Traditional 12/03/2018SE
K163073Sol-Care Safety Blood Collection Needle with and without Pre-Attached HolderJKA · Traditional 05/19/2017SE

Questions and answers

When was SOL-GUARD Safety Pull Button Collection Set cleared by the FDA?

SOL-GUARD Safety Pull Button Collection Set (K213718) received a 510(k) decision of Substantially Equivalent on August 30, 2022, 279 days after the submission was received.

What is the product code of K213718?

The FDA product code is JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection, a Class II (moderate risk) device regulated under 21 CFR 862.1675.