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FDA 510(k)

Aesculap Slim Clip Applier

K-Number: K211572 · 2021-12-13

ApplicantAesculap, Inc.
Decision Date2021-12-13
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Aesculap Slim Clip Applier is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2021-12-13 under 510(k) 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. The listed applicant is Aesculap, Inc.. The 510(k) number is K211572.

When did Aesculap Slim Clip Applier receive FDA 510(k) clearance?

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

Who is the listed applicant for Aesculap Slim Clip Applier?

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

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

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

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: HCI)

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.

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

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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