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FDA 510(k)

Cautery Protective Actuation System (CPAS)

K-Number: K232407 · 2023-10-06

ApplicantSafer Surgeries Medical Devices, LLC
Decision Date2023-10-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cautery Protective Actuation System (CPAS) is a medical device manufactured by Safer Surgeries Medical Devices, LLC. It received FDA 510(k) clearance on 2023-10-06 under approval number K232407. 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 Cautery Protective Actuation System (CPAS)?

Cautery Protective Actuation System (CPAS) is a medical device that received FDA 510(k) clearance on 2023-10-06. It is manufactured by Safer Surgeries Medical Devices, LLC. The 510(k) number is K232407.

When was Cautery Protective Actuation System (CPAS) approved by the FDA?

Cautery Protective Actuation System (CPAS) received FDA 510(k) clearance on 2023-10-06, under approval number K232407.

What company makes Cautery Protective Actuation System (CPAS)?

Cautery Protective Actuation System (CPAS) is manufactured by Safer Surgeries Medical Devices, LLC.

What is the FDA product code for Cautery Protective Actuation System (CPAS)?

The FDA product code for Cautery Protective Actuation System (CPAS) is GEI.

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Official Source

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