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FDA 510(k)

Aesculap Caiman 5 Seal and Cut Technology System

K-Number: K202938 · 2020-10-30

ApplicantAesculap, Inc.
Decision Date2020-10-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Aesculap Caiman 5 Seal and Cut Technology System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-10-30 under 510(k) number K202938. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aesculap Caiman 5 Seal and Cut Technology System?

Aesculap Caiman 5 Seal and Cut Technology System is a medical device that received FDA 510(k) clearance on 2020-10-30. The listed applicant is Aesculap, Inc.. The 510(k) number is K202938.

When did Aesculap Caiman 5 Seal and Cut Technology System receive FDA 510(k) clearance?

Aesculap Caiman 5 Seal and Cut Technology System received FDA 510(k) clearance on 2020-10-30, under 510(k) number K202938.

Who is the listed applicant for Aesculap Caiman 5 Seal and Cut Technology System?

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 Caiman 5 Seal and Cut Technology System?

The FDA product code for Aesculap Caiman 5 Seal and Cut Technology System is GEI.

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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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