Inrad 601415

• FDA 510(k) K981721 decided 28 Jul 1998 Active
• FDA GUDID UDI-DI 00817295020879 listed 1 Dec 2016 Listed

1. 28 Jul 1998 Cleared FDA 510(k) K981721
2. 1 Dec 2016 Listed FDA GUDID 00817295020879

Trade name

Inrad

Generic name

Soft-tissue biopsy needle, single-use

Model / reference

601415

Primary DI / UDI-DI

00817295020879

510(k) Number

K981721 ↗

FDA product code

KNW

GMDN term

Soft-tissue biopsy needle, single-use

Device class

Class II

Regulation number

876.1075

GUDID distribution status

In Commercial Distribution

Category: Soft-tissue biopsy needle, single-use

Other devices filed under FDA product code KNW (Instrument, Biopsy).

• Pink Achieve™ 10884450444297 BCA1215/B by Merit Medical Systems, Inc.
• Osteo-Site Bone Biopsy Needle, Osteo-Site Bone Biopsy Needle Set by COOK INCORPORATED
• Co-Axial Introducer Needle MCXS1816AX by Argon Medical Devices, Inc.
• Bard Monopty Disposable Core Biopsy Instrument by C. R. Bard, Inc.
• Jamshidi Marrow Acquisition Cradle by Allegiance Healthcare Corp.
• Modified Biopsy Needle by Biopsys Medical, Inc.
• Bone Marrow Harvest Needle BMHN1104VX by Argon Medical Devices, Inc.
• ACHIEVE PROGRAMMABLE AUOMATED BIOPSY SYSTEMS by CAREFUSION
• CorVocet™ 00884450476406 CORCA1815SB/B by Merit Medical Systems, Inc.
• BMN J TYPE J0810 by H.S. HOSPITAL SERVICE SPA

• Inrad 53220

  Class I

  FDA 510(k) K813368 Active Cleared 5 Jan 1982 GUDID on market

• Inrad 53222

  Class I

  FDA 510(k) K813368 Active Cleared 5 Jan 1982 GUDID on market

• Inrad 53218

  Class I

  FDA 510(k) K813368 Active Cleared 5 Jan 1982 GUDID on market

• Inrad 41222

  Class I

  FDA 510(k) K813368 Active Cleared 5 Jan 1982 GUDID on market

See all devices from Inrad →