AESCULAP AXIAL CLIP APPLIER— 510(k) K984109

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K984109 for AESCULAP AXIAL CLIP APPLIER, Substantially Equivalent on 1999-02-12. 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: 1998-11-17
Decision date: 1999-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, CA, 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
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 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.