Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation

K-Number: K242266 · 2024-10-21

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

Device Summary

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation is a medical device manufactured by Stryker Instruments. It received FDA 510(k) clearance on 2024-10-21 under approval 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. It is manufactured by Stryker Instruments. The 510(k) number is K242266.

When was PhotonBlade 3; PhotonBlade 3 Smoke Evacuation approved by the FDA?

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

What company makes PhotonBlade 3; PhotonBlade 3 Smoke Evacuation?

PhotonBlade 3; PhotonBlade 3 Smoke Evacuation is manufactured by Stryker Instruments.

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.

Related Clinical Trials

Other Devices by Stryker Instruments

View all 19 devices →

Related Devices (Code: GEI)

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.