LAPAROSCOPIC VESSEL ARTICULATOR— 510(k) K911475

Name: FDA 510(k) clearance K911475
Creator: U.S. Food and Drug Administration
Published: 1991-07-02

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K911475 for LAPAROSCOPIC VESSEL ARTICULATOR, Substantially Equivalent on 1991-07-02. Applicant: United States Endoscopy Group, Inc.. Device class: 2.

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code DWP
Device class: Class 2
Regulation: 21 CFR 870.4475
Advisory panel: Cardiovascular
Date received: 1991-04-04
Decision date: 1991-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DWP

view all

K220981 — SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe2023-04-20
K183438 — Geomed Vascular Dilators2019-09-03
K163524 — Vessel Dilator2017-06-29
K130896 — VASCULAR PROBE, VASCULAR PROBE ES2013-04-24
K100518 — INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-70542010-08-31

More clearances from United States Endoscopy Group, Inc.

view all

K192265 — gi-4000 Electrosurgical Generator2020-05-21
K200745 — Lariat, Hot/Cold Snare2020-04-21
K192059 — Bio Guard Air/Water & Suction Valves2019-09-17
K191559 — AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM2019-08-01
K182909 — Roth Net Retriever Product Line2018-11-21

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