Specialty Needles (Spinal Needle, Pencil Point Spinal Needle, Epidural Needle)

FDA 510(k) K061394 · Busse Hospital Disposables, Inc.

Substantially Equivalent

510(k) numberK061394

Submission

Device name
Specialty Needles (Spinal Needle, Pencil Point Spinal Needle, Epidural Needle)
Applicant
Busse Hospital Disposables, Inc.
Hauppauge, NY, US
Received
May 19, 2006
Decision date
September 6, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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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Questions and answers

When was Specialty Needles (Spinal Needle, Pencil Point Spinal Needle, Epidural Needle) cleared by the FDA?

Specialty Needles (Spinal Needle, Pencil Point Spinal Needle, Epidural Needle) (K061394) received a 510(k) decision of Substantially Equivalent on September 6, 2006, 110 days after the submission was received.

What is the product code of K061394?

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