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FDA 510(k)

AESCULAP ENDOSCOPIC CLIP SYTEM

K-Number: K080753 · 2008-04-02

ApplicantAesculap, Inc.
Decision Date2008-04-02
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP ENDOSCOPIC CLIP SYTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2008-04-02 under 510(k) number K080753. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP ENDOSCOPIC CLIP SYTEM?

AESCULAP ENDOSCOPIC CLIP SYTEM is a medical device that received FDA 510(k) clearance on 2008-04-02. The listed applicant is Aesculap, Inc.. The 510(k) number is K080753.

When did AESCULAP ENDOSCOPIC CLIP SYTEM receive FDA 510(k) clearance?

AESCULAP ENDOSCOPIC CLIP SYTEM received FDA 510(k) clearance on 2008-04-02, under 510(k) number K080753.

Who is the listed applicant for AESCULAP ENDOSCOPIC CLIP SYTEM?

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 ENDOSCOPIC CLIP SYTEM?

The FDA product code for AESCULAP ENDOSCOPIC CLIP SYTEM is FZP.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: FZP)

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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