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FDA 510(k)

STRYKER SCOPE/INSTRUMENT HOLDER

K-Number: K060085 · 2006-04-27

ApplicantStryker Endoscopy
Decision Date2006-04-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER SCOPE/INSTRUMENT HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2006-04-27 under 510(k) number K060085. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER SCOPE/INSTRUMENT HOLDER?

STRYKER SCOPE/INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 2006-04-27. The listed applicant is Stryker Endoscopy. The 510(k) number is K060085.

When did STRYKER SCOPE/INSTRUMENT HOLDER receive FDA 510(k) clearance?

STRYKER SCOPE/INSTRUMENT HOLDER received FDA 510(k) clearance on 2006-04-27, under 510(k) number K060085.

Who is the listed applicant for STRYKER SCOPE/INSTRUMENT HOLDER?

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 SCOPE/INSTRUMENT HOLDER?

The FDA product code for STRYKER SCOPE/INSTRUMENT HOLDER is GCJ.

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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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