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FDA 510(k)

HARMONIC 700 Shears

K-Number: K221790 · 2023-02-28

ApplicantEthicon Endo-Surgery, LLC
Decision Date2023-02-28
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

HARMONIC 700 Shears is a medical device manufactured by Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2023-02-28 under approval number K221790. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARMONIC 700 Shears?

HARMONIC 700 Shears is a medical device that received FDA 510(k) clearance on 2023-02-28. It is manufactured by Ethicon Endo-Surgery, LLC. The 510(k) number is K221790.

When was HARMONIC 700 Shears approved by the FDA?

HARMONIC 700 Shears received FDA 510(k) clearance on 2023-02-28, under approval number K221790.

What company makes HARMONIC 700 Shears?

HARMONIC 700 Shears is manufactured by Ethicon Endo-Surgery, LLC.

What is the FDA product code for HARMONIC 700 Shears?

The FDA product code for HARMONIC 700 Shears is LFL.

Related Clinical Trials

NCT06608485 A Study of HARMONIC 700 Shears With Advanced Hemostasis in Pediatric and Adult Surgical Procedures RECRUITING

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Related Devices (Code: LFL)

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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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