Mediziv Spinal Needle Set

FDA 510(k) K925831 · Medicia Medical Products

Substantially Equivalent

510(k) numberK925831

Submission

Device name
Mediziv Spinal Needle Set
Applicant
Medicia Medical Products
Tel-Aviv 62264 Israel, IL
Received
November 16, 1992
Decision date
July 16, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BSP – Needle, Conduction, Anesthetic (W/Wo Introducer)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5150
Specialty
Anesthesiology

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K250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PunctureBSP · Traditional PAJUNK GmbH Medizintechnologie06/25/2025SE
K243525SonoTAP and SonoTAP IIBSP · Traditional PAJUNK GmbH Medizintechnologie03/24/2025SE
K241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyBSP · Traditional PAJUNK GmbH Medizintechnologie11/22/2024SE
K241954SonoBlock; SonoBlock IIBSP · Traditional PAJUNK GmbH Medizintechnologie09/11/2024SE
K240253Reach NeedleBSP · Traditional Aerin Medical, Inc.03/21/2024SE
K212982Medispine - Spinal Needle, Glospine - Spinal NeedleBSP · Traditional Global Medikit Limited07/29/2022SE
K211085BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural NeedleBSP · Traditional Becton, Dickinson and Company07/01/2022SE
K210978BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer NeedleBSP · Traditional Becton, Dickinson and Company12/22/2021SE

More from Becton, Dickinson and Company

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Questions and answers

When was Mediziv Spinal Needle Set cleared by the FDA?

Mediziv Spinal Needle Set (K925831) received a 510(k) decision of Substantially Equivalent on July 16, 1993, 242 days after the submission was received.

What is the product code of K925831?

The FDA product code is BSP – Needle, Conduction, Anesthetic (W/Wo Introducer), a Class II (moderate risk) device regulated under 21 CFR 868.5150.