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FDA 510(k)

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER

K-Number: K940130 · 1994-03-10

ApplicantStryker Corp.
Decision Date1994-03-10
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K940130. 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 STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER?

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Stryker Corp.. The 510(k) number is K940130.

When did STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER receive FDA 510(k) clearance?

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER received FDA 510(k) clearance on 1994-03-10, under 510(k) number K940130.

Who is the listed applicant for STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER?

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

What is the FDA product code for STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER?

The FDA product code for STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER is FPP.

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Other records listing Stryker Corp. as applicant

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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.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, Inc.K924669FERNO-WASHINGTON BASKET STRETCHER, MODEL 71-WFerno

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.

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