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)

IRSG I-MOVER FOR BEDS

K-Number: K072598 · 2008-04-14

ApplicantInternational Retail Services Group, LLC
Decision Date2008-04-14
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IRSG I-MOVER FOR BEDS is the device name listed in this FDA 510(k) record. The listed applicant is International Retail Services Group, LLC. It received FDA 510(k) clearance on 2008-04-14 under 510(k) number K072598. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRSG I-MOVER FOR BEDS?

IRSG I-MOVER FOR BEDS is a medical device that received FDA 510(k) clearance on 2008-04-14. The listed applicant is International Retail Services Group, LLC. The 510(k) number is K072598.

When did IRSG I-MOVER FOR BEDS receive FDA 510(k) clearance?

IRSG I-MOVER FOR BEDS received FDA 510(k) clearance on 2008-04-14, under 510(k) number K072598.

Who is the listed applicant for IRSG I-MOVER FOR BEDS?

The FDA 510(k) record lists International Retail Services Group, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IRSG I-MOVER FOR BEDS?

The FDA product code for IRSG I-MOVER FOR BEDS is FPO.

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: FPO)

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.

K113598POWER-LOAD COT FASTENER SYSTEMStryker MedicalK972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K961437WHEELED STRETCHERHill-Rom, Inc.K952447HILL-ROM AMBULATORY CARE PROCEDURAL STRETCHERHill-Rom, 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.

↑