WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE— 510(k) K981470

Name: FDA 510(k) clearance K981470
Creator: U.S. Food and Drug Administration
Published: 1998-06-19

Substantially Equivalent

Worldwide Medical Technologies, LLC

FDA 510(k) clearance K981470 for WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE, Substantially Equivalent on 1998-06-19. Applicant: Worldwide Medical Technologies, LLC. Device class: 2.

Clearance details

Applicant: Worldwide Medical Technologies, LLC
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1998-04-23
Decision date: 1998-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodbury, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZH

view all

K203509 — SMART FINDER2021-07-14
K202294 — Affirm Contrast Biopsy2020-10-05
K191495 — Biopsy Positioner2019-07-03
K161575 — Affirm Lateral Arm Upright Biopsy Accessory2016-08-10
K161920 — Comfort Cover2016-07-15

More clearances from Worldwide Medical Technologies, LLC

view all

K062214 — BRACHYSCIENCES STRANDPORT2007-03-01
K023179 — READI-STRAND, MODEL PSSTRAND2003-07-02
K022705 — READI-STRAND, MODEL PSSTRAND2003-06-09
K022389 — READI-LOAD SYSTEM, MODEL PSS 1820RL2003-05-06
K020641 — SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 0012002-10-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.