Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE

K-Number: K081031 · 2008-05-05

ApplicantAesculap, Inc.
Decision Date2008-05-05
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2008-05-05 under 510(k) number K081031. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE?

ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE is a medical device that received FDA 510(k) clearance on 2008-05-05. The listed applicant is Aesculap, Inc.. The 510(k) number is K081031.

When did ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE receive FDA 510(k) clearance?

ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE received FDA 510(k) clearance on 2008-05-05, under 510(k) number K081031.

Who is the listed applicant for ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE?

The FDA 510(k) record lists Aesculap, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE?

The FDA product code for ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE is FZP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Aesculap, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

View all 195 devices →

Related Devices (Code: FZP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260677Vessel Closure Device (VCD177213P)Vcd Medical S.R.L.K254231Inno-Hook™ Disposable Clip Appliers (Ligating Clips) and Inno-Hook™ Ligating ClipsTaiwan Surgical CorporationK253781InnoClip Clip ApplierTaiwan Surgical CorporationK253903InnoClip Disposable Clip ApplierTaiwan Surgical CorporationK250643Disposable Polymer Ligation ClipsHangzhou Kangji Medical Instrument Co., Ltd.K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsTeleflex Medical

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑