PERNECZKY CLIP APPLIER/REMOVER— 510(k) K954658

Name: FDA 510(k) clearance K954658
Creator: U.S. Food and Drug Administration
Published: 1996-10-08

Substantially Equivalent

Von Zeppelin GmbH

FDA 510(k) clearance K954658 for PERNECZKY CLIP APPLIER/REMOVER, Substantially Equivalent on 1996-10-08. Applicant: Von Zeppelin GmbH. Device class: 2.

Clearance details

Applicant: Von Zeppelin GmbH
Product code: Code HCI
Device class: Class 2
Regulation: 21 CFR 882.4175
Advisory panel: Neurology
Date received: 1995-10-10
Decision date: 1996-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pullach, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code HCI

view all

K221524 — Sugita AVM Microclip Applier2022-06-24
K211572 — Aesculap Slim Clip Applier2021-12-13
K180914 — Aesculap Slim Clip Applier2018-04-17
K173271 — Aesculap Slim Clip Applier Forceps2017-11-10
K010910 — MEDICON YASARGIL CLIP APPLYING FORCEPS2001-08-01

More clearances from Von Zeppelin GmbH

view all

K013091 — ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM2002-01-25
K903151 — INTERVERTEBRAL DISC RONGEUR1990-12-11
K901312 — PERNECZKY ANEURYSM CLIP1990-08-17
K901313 — INSTRUMENTS FOR NEUROLOGICAL SURGERY1990-07-23

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