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)

DANIEL ORTHO BED LIFT AC

K-Number: K862738 · 1986-07-29

ApplicantRadco
Decision Date1986-07-29
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DANIEL ORTHO BED LIFT AC is the device name listed in this FDA 510(k) record. The listed applicant is Radco. It received FDA 510(k) clearance on 1986-07-29 under 510(k) number K862738. 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 DANIEL ORTHO BED LIFT AC?

DANIEL ORTHO BED LIFT AC is a medical device that received FDA 510(k) clearance on 1986-07-29. The listed applicant is Radco. The 510(k) number is K862738.

When did DANIEL ORTHO BED LIFT AC receive FDA 510(k) clearance?

DANIEL ORTHO BED LIFT AC received FDA 510(k) clearance on 1986-07-29, under 510(k) number K862738.

Who is the listed applicant for DANIEL ORTHO BED LIFT AC?

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

What is the FDA product code for DANIEL ORTHO BED LIFT AC?

The FDA product code for DANIEL ORTHO BED LIFT AC 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

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.

↑