Inrad 661710

• FDA 510(k) K981721 decided 28 Jul 1998 Active
• FDA GUDID UDI-DI 00817295021043 listed 1 Dec 2016 Listed

1. 28 Jul 1998 Cleared FDA 510(k) K981721
2. 1 Dec 2016 Listed FDA GUDID 00817295021043

Trade name

Inrad

Generic name

Soft-tissue biopsy needle, single-use

Model / reference

661710

Primary DI / UDI-DI

00817295021043

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).

• ACECUT SUTOMATIC BIOPSY SYSTEM by Meadox Surgimed, Inc.
• CorVocet™ 00884450476383 CORCA1810SB/B by Merit Medical Systems, Inc.
• Sanarus Centrica Core Tissue Biopsy System by Sanarus Medical, Inc.
• TRU-CORE NEEDLE SET by Ideamatrix
• Mammotome MR MRU08S by Devicor Medical Products, Inc.
• Pro-Mag™ Biopsy Needle 765016160 by Argon Medical Devices, Inc.
• SuperCore™ Biopsy Instrument 701120060 by Argon Medical Devices, Inc.
• BMRI Soft Tissue Biopsy Needle by Bio-Medical Resources, Inc.
• Presto Breast Biopsy Device by Sontina Medical, LLC
• 15MM SITESELECT BREAST BIOPSY DEVICE, 10 MM SITESELECT BREAST BIOPSY DEVICE, 5MM SITESELECT BREAST BIOPSY DEVICE by Imagyn Surgical

• 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 →