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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 a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2020-10-30 under approval 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. It is manufactured by Aesculap, Inc.. The 510(k) number is K202938.

When was Aesculap Caiman 5 Seal and Cut Technology System approved by the FDA?

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

What company makes Aesculap Caiman 5 Seal and Cut Technology System?

Aesculap Caiman 5 Seal and Cut Technology System is manufactured by Aesculap, Inc..

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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Related PubMed Literature

PMID: 41887630 Capacity building for ethical use of artificial intelligence in health: protocol for a scoping review of training initiatives and gaps in Africa. BMJ open (2026) PMID: 41054198 Relevant domains for health technology assessment of medical device reimbursement in Brazil's unified health system: a survey and Delphi panel study on stakeholder preferences. International journal of technology assessment in health care (2025) PMID: 40837401 Mining and evaluation of security alert signals of neuroprotective agents based on the Jinan adverse event reporting system database: a retrospective study. Frontiers in pharmacology (2025) PMID: 40407411 A data augmentation approach for an automatic speech recognition system using laser Doppler vibrometer technology. JASA express letters (2025)

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Official Source

View on FDA Database →

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