Acu-Micro-Needle

FDA 510(k) K874024 · Acuderm, Inc.

Substantially Equivalent

510(k) numberK874024

Submission

Device name
Acu-Micro-Needle
Applicant
Acuderm, Inc.
Ft. Lauderdale, FL, US
Received
October 2, 1987
Decision date
November 23, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Ningbo Medsun Medical Co., Ltd.

510(k)DeviceDecision
K933516Acu-E PunchLRY · Traditional 03/24/1994SE
K933265Acu-Dispo-Ce(Tm)MDM · Traditional 03/07/1994SE
K933137Acu-Suture KitLRO · Traditional 02/22/1994SE
K930043Acu-EvacFYD · Traditional 02/09/1994SE
K933866Acu-Hemostatic RingMDM · Traditional 12/01/1993SE
K915000Acu-GuardGEX · Traditional 01/27/1992SE
K891334Acu-CuretteFZS · Traditional 04/11/1989SE
K854877Acu-Syringe W/Wo NeedlesFMF · Traditional 02/19/1986SE
K832583Sabouraud Dextrose AgarJSJ · Traditional 09/12/1983SE
K832582Mycosel AgarJSJ · Traditional 09/12/1983SE

Questions and answers

When was Acu-Micro-Needle cleared by the FDA?

Acu-Micro-Needle (K874024) received a 510(k) decision of Substantially Equivalent on November 23, 1987, 52 days after the submission was received.

What is the product code of K874024?

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