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FDA 510(k)

PADLOCK CLIP EFTR Kit (00713229)

K-Number: K240274 · 2024-09-17

ApplicantSTERIS Corporation
Decision Date2024-09-17
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PADLOCK CLIP EFTR Kit (00713229) is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2024-09-17 under 510(k) number K240274. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PADLOCK CLIP EFTR Kit (00713229)?

PADLOCK CLIP EFTR Kit (00713229) is a medical device that received FDA 510(k) clearance on 2024-09-17. The listed applicant is STERIS Corporation. The 510(k) number is K240274.

When did PADLOCK CLIP EFTR Kit (00713229) receive FDA 510(k) clearance?

PADLOCK CLIP EFTR Kit (00713229) received FDA 510(k) clearance on 2024-09-17, under 510(k) number K240274.

Who is the listed applicant for PADLOCK CLIP EFTR Kit (00713229)?

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

What is the FDA product code for PADLOCK CLIP EFTR Kit (00713229)?

The FDA product code for PADLOCK CLIP EFTR Kit (00713229) is PKL.

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Related Devices (Code: PKL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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