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)

YASARGIL, CASPAR, VARIO CLIP APPLIERS

K-Number: K940970 · 1995-01-24

ApplicantAesculap, Inc.
Decision Date1995-01-24
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

YASARGIL, CASPAR, VARIO CLIP APPLIERS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K940970. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YASARGIL, CASPAR, VARIO CLIP APPLIERS?

YASARGIL, CASPAR, VARIO CLIP APPLIERS is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Aesculap, Inc.. The 510(k) number is K940970.

When did YASARGIL, CASPAR, VARIO CLIP APPLIERS receive FDA 510(k) clearance?

YASARGIL, CASPAR, VARIO CLIP APPLIERS received FDA 510(k) clearance on 1995-01-24, under 510(k) number K940970.

Who is the listed applicant for YASARGIL, CASPAR, VARIO CLIP APPLIERS?

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 YASARGIL, CASPAR, VARIO CLIP APPLIERS?

The FDA product code for YASARGIL, CASPAR, VARIO CLIP APPLIERS is HCI.

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: HCI)

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.

K221524Sugita AVM Microclip ApplierMizuho America, Inc.K211572Aesculap Slim Clip ApplierAesculap, Inc.K180914Aesculap Slim Clip ApplierAesculap, Inc.K173271Aesculap Slim Clip Applier ForcepsAesculap, Inc.K010910MEDICON YASARGIL CLIP APPLYING FORCEPSMedicon EGK994191SPETZLER ROUND HANDLE APPLIERS, MODELS C-3753, C-3753T, C-3754, C-3754TNmt Medical, Inc.

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.

↑