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FDA 510(k)

CAIMAN SEAL AND CUT TECHNOLOGY

K-Number: K130596 · 2013-03-22

ApplicantAesculap, Inc.
Decision Date2013-03-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAIMAN SEAL AND CUT TECHNOLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2013-03-22 under 510(k) number K130596. 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 CAIMAN SEAL AND CUT TECHNOLOGY?

CAIMAN SEAL AND CUT TECHNOLOGY is a medical device that received FDA 510(k) clearance on 2013-03-22. The listed applicant is Aesculap, Inc.. The 510(k) number is K130596.

When did CAIMAN SEAL AND CUT TECHNOLOGY receive FDA 510(k) clearance?

CAIMAN SEAL AND CUT TECHNOLOGY received FDA 510(k) clearance on 2013-03-22, under 510(k) number K130596.

Who is the listed applicant for CAIMAN SEAL AND CUT TECHNOLOGY?

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 CAIMAN SEAL AND CUT TECHNOLOGY?

The FDA product code for CAIMAN SEAL AND CUT TECHNOLOGY 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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