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FDA 510(k)

STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS

K-Number: K061225 · 2006-09-14

ApplicantStryker Corp.
Decision Date2006-09-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2006-09-14 under 510(k) number K061225. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS?

STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS is a medical device that received FDA 510(k) clearance on 2006-09-14. The listed applicant is Stryker Corp.. The 510(k) number is K061225.

When did STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS receive FDA 510(k) clearance?

STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS received FDA 510(k) clearance on 2006-09-14, under 510(k) number K061225.

Who is the listed applicant for STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS?

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 DISPOSABLE LAPAROSCOPIC SCISSORS?

The FDA product code for STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS is GEI.

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Related Devices (Code: GEI)

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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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