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)

SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART

K-Number: K895740 · 1990-02-22

ApplicantLumex, Inc.
Decision Date1990-02-22
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART is the device name listed in this FDA 510(k) record. The listed applicant is Lumex, Inc.. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K895740. 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 SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART?

SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Lumex, Inc.. The 510(k) number is K895740.

When did SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART receive FDA 510(k) clearance?

SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART received FDA 510(k) clearance on 1990-02-22, under 510(k) number K895740.

Who is the listed applicant for SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART?

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

What is the FDA product code for SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART?

The FDA product code for SHOWER CHAIRS;BED/STRETCHER;LINEN & UTILITY CART 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

Other records listing Lumex, 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.

K963674LUMEX AIRK962123AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEMK953675ALTADYNEK945175MECHANICAL WHEELCHAIR 890.3850K945257577ES (ERGOSENSE)K944574LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)

View all 8 devices →

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 MedicalK072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLCK972528DYNA 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.

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.

↑