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FDA 510(k)

STRYKER L3 HYDROLERT

K-Number: K022248 · 2002-08-06

ApplicantStryker Endoscopy
Decision Date2002-08-06
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER L3 HYDROLERT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2002-08-06 under 510(k) number K022248. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER L3 HYDROLERT?

STRYKER L3 HYDROLERT is a medical device that received FDA 510(k) clearance on 2002-08-06. The listed applicant is Stryker Endoscopy. The 510(k) number is K022248.

When did STRYKER L3 HYDROLERT receive FDA 510(k) clearance?

STRYKER L3 HYDROLERT received FDA 510(k) clearance on 2002-08-06, under 510(k) number K022248.

Who is the listed applicant for STRYKER L3 HYDROLERT?

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 L3 HYDROLERT?

The FDA product code for STRYKER L3 HYDROLERT is FLN.

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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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