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FDA 510(k)

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation

K-Number: K242266 · 2024-10-21

ApplicantStryker Instruments
Decision Date2024-10-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2024-10-21 under 510(k) number K242266. 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 PhotonBlade 3; PhotonBlade 3 Smoke Evacuation?

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation is a medical device that received FDA 510(k) clearance on 2024-10-21. The listed applicant is Stryker Instruments. The 510(k) number is K242266.

When did PhotonBlade 3; PhotonBlade 3 Smoke Evacuation receive FDA 510(k) clearance?

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation received FDA 510(k) clearance on 2024-10-21, under 510(k) number K242266.

Who is the listed applicant for PhotonBlade 3; PhotonBlade 3 Smoke Evacuation?

The FDA 510(k) record lists Stryker Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PhotonBlade 3; PhotonBlade 3 Smoke Evacuation?

The FDA product code for PhotonBlade 3; PhotonBlade 3 Smoke Evacuation is 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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