Aesculap Slim Clip Applier— 510(k) K180914

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K180914 for Aesculap Slim Clip Applier, Substantially Equivalent on 2018-04-17. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HCI
Device class: Class 2
Regulation: 21 CFR 882.4175
Advisory panel: Neurology
Date received: 2018-04-09
Decision date: 2018-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HCI

K221524 — Sugita AVM Microclip Applier2022-06-24
K211572 — Aesculap Slim Clip Applier2021-12-13
K173271 — Aesculap Slim Clip Applier Forceps2017-11-10
K010910 — MEDICON YASARGIL CLIP APPLYING FORCEPS2001-08-01
K994191 — SPETZLER ROUND HANDLE APPLIERS, MODELS C-3753, C-3753T, C-3754, C-3754T2000-02-08

More clearances from Aesculap, Inc.

K242762 — Aesculap Aicon® Series Container System2025-05-13
K242003 — XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set2024-12-16
K223596 — SQ.line KERRISON2023-06-29
K214041 — Aesculap AICON Container2022-12-30
K203739 — ELAN 4 Electro Motor System2021-08-24

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