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FDA 510(k)

HAND CARRIED STRETCHER

K-Number: K911765 · 1991-06-14

ApplicantL.E. Phillips Career Development Center, Inc.
Decision Date1991-06-14
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HAND CARRIED STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is L.E. Phillips Career Development Center, Inc.. It received FDA 510(k) clearance on 1991-06-14 under 510(k) number K911765. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND CARRIED STRETCHER?

HAND CARRIED STRETCHER is a medical device that received FDA 510(k) clearance on 1991-06-14. The listed applicant is L.E. Phillips Career Development Center, Inc.. The 510(k) number is K911765.

When did HAND CARRIED STRETCHER receive FDA 510(k) clearance?

HAND CARRIED STRETCHER received FDA 510(k) clearance on 1991-06-14, under 510(k) number K911765.

Who is the listed applicant for HAND CARRIED STRETCHER?

The FDA 510(k) record lists L.E. Phillips Career Development Center, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAND CARRIED STRETCHER?

The FDA product code for HAND CARRIED STRETCHER is FPP.

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: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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