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FDA 510(k)

STRYKER ARTHROSCOPIC ACCESSORIES

K-Number: K930224 · 1994-06-30

ApplicantStryker Corp.
Decision Date1994-06-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER ARTHROSCOPIC ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1994-06-30 under 510(k) number K930224. 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 ARTHROSCOPIC ACCESSORIES?

STRYKER ARTHROSCOPIC ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-06-30. The listed applicant is Stryker Corp.. The 510(k) number is K930224.

When did STRYKER ARTHROSCOPIC ACCESSORIES receive FDA 510(k) clearance?

STRYKER ARTHROSCOPIC ACCESSORIES received FDA 510(k) clearance on 1994-06-30, under 510(k) number K930224.

Who is the listed applicant for STRYKER ARTHROSCOPIC ACCESSORIES?

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 ARTHROSCOPIC ACCESSORIES?

The FDA product code for STRYKER ARTHROSCOPIC ACCESSORIES is GCJ.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: 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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