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FDA 510(k)

TCM ENDO 20

K-Number: K081191 · 2008-08-07

ApplicantNOUVAG AG
Decision Date2008-08-07
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TCM ENDO 20 is the device name listed in this FDA 510(k) record. The listed applicant is NOUVAG AG. It received FDA 510(k) clearance on 2008-08-07 under 510(k) number K081191. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TCM ENDO 20?

TCM ENDO 20 is a medical device that received FDA 510(k) clearance on 2008-08-07. The listed applicant is NOUVAG AG. The 510(k) number is K081191.

When did TCM ENDO 20 receive FDA 510(k) clearance?

TCM ENDO 20 received FDA 510(k) clearance on 2008-08-07, under 510(k) number K081191.

Who is the listed applicant for TCM ENDO 20?

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

What is the FDA product code for TCM ENDO 20?

The FDA product code for TCM ENDO 20 is EKX.

Other records listing NOUVAG AG as applicant

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.

View all 12 devices →

Related Devices (Code: EKX)

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.

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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