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FDA 510(k)

STRYKER LAPAROSCOPE

K-Number: K910132 · 1991-02-21

ApplicantStryker Corp.
Decision Date1991-02-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STRYKER LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K910132. 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 LAPAROSCOPE?

STRYKER LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Stryker Corp.. The 510(k) number is K910132.

When did STRYKER LAPAROSCOPE receive FDA 510(k) clearance?

STRYKER LAPAROSCOPE received FDA 510(k) clearance on 1991-02-21, under 510(k) number K910132.

Who is the listed applicant for STRYKER LAPAROSCOPE?

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 LAPAROSCOPE?

The FDA product code for STRYKER LAPAROSCOPE is GCJ.

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Other records listing Stryker Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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