FDA 510(k)

Aesculap Slim Clip Applier

K-Number: K211572 · 2021-12-13

Decision Date2021-12-13

Product CodeHCI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Aesculap Slim Clip Applier is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2021-12-13 under approval number K211572. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aesculap Slim Clip Applier?

Aesculap Slim Clip Applier is a medical device that received FDA 510(k) clearance on 2021-12-13. It is manufactured by Aesculap, Inc.. The 510(k) number is K211572.

When was Aesculap Slim Clip Applier approved by the FDA?

Aesculap Slim Clip Applier received FDA 510(k) clearance on 2021-12-13, under approval number K211572.

What company makes Aesculap Slim Clip Applier?

Aesculap Slim Clip Applier is manufactured by Aesculap, Inc..

What is the FDA product code for Aesculap Slim Clip Applier?

The FDA product code for Aesculap Slim Clip Applier is HCI.

Other Devices by Aesculap, Inc.

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Related Devices (Code: HCI)

K173271Aesculap Slim Clip Applier ForcepsAesculap, Inc. K180914Aesculap Slim Clip ApplierAesculap, Inc. K221524Sugita AVM Microclip ApplierMizuho America, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.