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FDA 510(k)

STRYKER POWERED STRETCHER

K-Number: K942948 · 1995-01-24

ApplicantStryker Corp.
Decision Date1995-01-24
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER POWERED 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 1995-01-24 under 510(k) number K942948. 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 STRYKER POWERED STRETCHER?

STRYKER POWERED STRETCHER is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Stryker Corp.. The 510(k) number is K942948.

When did STRYKER POWERED STRETCHER receive FDA 510(k) clearance?

STRYKER POWERED STRETCHER received FDA 510(k) clearance on 1995-01-24, under 510(k) number K942948.

Who is the listed applicant for STRYKER POWERED 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 POWERED STRETCHER?

The FDA product code for STRYKER POWERED STRETCHER is FPO.

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Other records listing Stryker Corp. 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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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.

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