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FDA 510(k)

LIFE LITE EMERGENCY STRETCHER

K-Number: K920805 · 1992-05-22

ApplicantDesign Principles, Inc.
Decision Date1992-05-22
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFE LITE EMERGENCY STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Design Principles, Inc.. It received FDA 510(k) clearance on 1992-05-22 under 510(k) number K920805. 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 LIFE LITE EMERGENCY STRETCHER?

LIFE LITE EMERGENCY STRETCHER is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Design Principles, Inc.. The 510(k) number is K920805.

When did LIFE LITE EMERGENCY STRETCHER receive FDA 510(k) clearance?

LIFE LITE EMERGENCY STRETCHER received FDA 510(k) clearance on 1992-05-22, under 510(k) number K920805.

Who is the listed applicant for LIFE LITE EMERGENCY STRETCHER?

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

What is the FDA product code for LIFE LITE EMERGENCY STRETCHER?

The FDA product code for LIFE LITE EMERGENCY STRETCHER is FPP.

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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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