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FDA 510(k)

ST5500 UNIVERSAL CARE STRETCHER

K-Number: K914543 · 1992-01-08

ApplicantLic Care, Inc.
Decision Date1992-01-08
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ST5500 UNIVERSAL CARE STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Lic Care, Inc.. It received FDA 510(k) clearance on 1992-01-08 under 510(k) number K914543. 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 ST5500 UNIVERSAL CARE STRETCHER?

ST5500 UNIVERSAL CARE STRETCHER is a medical device that received FDA 510(k) clearance on 1992-01-08. The listed applicant is Lic Care, Inc.. The 510(k) number is K914543.

When did ST5500 UNIVERSAL CARE STRETCHER receive FDA 510(k) clearance?

ST5500 UNIVERSAL CARE STRETCHER received FDA 510(k) clearance on 1992-01-08, under 510(k) number K914543.

Who is the listed applicant for ST5500 UNIVERSAL CARE STRETCHER?

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

What is the FDA product code for ST5500 UNIVERSAL CARE STRETCHER?

The FDA product code for ST5500 UNIVERSAL CARE STRETCHER 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 Lic Care, 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.

K914544BD6000 THE OPTIMA & BD5000 BIRTHING BED

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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