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FDA 510(k)

STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM

K-Number: K033135 · 2004-08-09

ApplicantStryker Endoscopy
Decision Date2004-08-09
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2004-08-09 under 510(k) number K033135. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM?

STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM is a medical device that received FDA 510(k) clearance on 2004-08-09. The listed applicant is Stryker Endoscopy. The 510(k) number is K033135.

When did STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM receive FDA 510(k) clearance?

STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM received FDA 510(k) clearance on 2004-08-09, under 510(k) number K033135.

Who is the listed applicant for STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM?

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

What is the FDA product code for STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM?

The FDA product code for STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM is KNS.

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Related Devices (Code: KNS)

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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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