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FDA 510(k)

STRYKER POWERED WHEELED STRETCHER

K-Number: K022309 · 2002-11-08

ApplicantStryker Corp.
Decision Date2002-11-08
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STRYKER POWERED WHEELED 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 2002-11-08 under 510(k) number K022309. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER POWERED WHEELED STRETCHER?

STRYKER POWERED WHEELED STRETCHER is a medical device that received FDA 510(k) clearance on 2002-11-08. The listed applicant is Stryker Corp.. The 510(k) number is K022309.

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

STRYKER POWERED WHEELED STRETCHER received FDA 510(k) clearance on 2002-11-08, under 510(k) number K022309.

Who is the listed applicant for STRYKER POWERED WHEELED 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 WHEELED STRETCHER?

The FDA product code for STRYKER POWERED WHEELED STRETCHER is INK.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: INK)

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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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