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)

BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540

K-Number: K033752 · 2003-12-12

ApplicantBruno Independent Living Aids, Inc.
Decision Date2003-12-12
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540 is the device name listed in this FDA 510(k) record. The listed applicant is Bruno Independent Living Aids, Inc.. It received FDA 510(k) clearance on 2003-12-12 under 510(k) number K033752. 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 BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540?

BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540 is a medical device that received FDA 510(k) clearance on 2003-12-12. The listed applicant is Bruno Independent Living Aids, Inc.. The 510(k) number is K033752.

When did BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540 receive FDA 510(k) clearance?

BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540 received FDA 510(k) clearance on 2003-12-12, under 510(k) number K033752.

Who is the listed applicant for BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540?

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

What is the FDA product code for BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540?

The FDA product code for BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540 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 Bruno Independent Living Aids, 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.

K113308BRUNO ELAN STAIRWAY ELEVATORK061514BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100K033829BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEM, MODEL CRE-2100K033438BRUNO ELECTRA-RIDE ELITE, MODEL SRE-2000K022509BRUNO ELECTRA-RIDE, MODEL SRE-2700K011227REGAL MOTOTRIZED 3 WHEELED VEHICLE

View all 12 devices →

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 MedicalK121560LEVANT, HOMEGLIDEThyssenkrupp Accessibility B.V.K121561FLOW2, SWINGThyssenkrupp Accessibility B.V.K113308BRUNO ELAN STAIRWAY ELEVATORBruno Independent Living Aids, Inc.K111858LIFTKAR PTSano Transportgeraete 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.

↑