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)

LEVANT, HOMEGLIDE

K-Number: K121560 · 2012-11-01

ApplicantThyssenkrupp Accessibility B.V.
Decision Date2012-11-01
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVANT, HOMEGLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Thyssenkrupp Accessibility B.V.. It received FDA 510(k) clearance on 2012-11-01 under 510(k) number K121560. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVANT, HOMEGLIDE?

LEVANT, HOMEGLIDE is a medical device that received FDA 510(k) clearance on 2012-11-01. The listed applicant is Thyssenkrupp Accessibility B.V.. The 510(k) number is K121560.

When did LEVANT, HOMEGLIDE receive FDA 510(k) clearance?

LEVANT, HOMEGLIDE received FDA 510(k) clearance on 2012-11-01, under 510(k) number K121560.

Who is the listed applicant for LEVANT, HOMEGLIDE?

The FDA 510(k) record lists Thyssenkrupp Accessibility B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVANT, HOMEGLIDE?

The FDA product code for LEVANT, HOMEGLIDE is ILK.

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 Thyssenkrupp Accessibility B.V. 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.

K121561FLOW2, SWING

Related Devices (Code: ILK)

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.

K240843GENESIS (MS-P02-GEN)Climbing Steps, Inc.K222818Xpedition ™ Powered Stair Chair (625700000000)Stryker MedicalK121561FLOW2, SWINGThyssenkrupp Accessibility B.V.K113308BRUNO ELAN STAIRWAY ELEVATORBruno Independent Living Aids, Inc.K111858LIFTKAR PTSano Transportgeraete GmbHK103122C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KGAat Alber Antriebstechnik GmbH

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.

↑