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FDA 510(k)

TENOLIG

K-Number: K060367 · 2006-08-09

ApplicantFournitures Hospitalieres Industrie
Decision Date2006-08-09
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TENOLIG is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2006-08-09 under 510(k) number K060367. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENOLIG?

TENOLIG is a medical device that received FDA 510(k) clearance on 2006-08-09. The listed applicant is Fournitures Hospitalieres Industrie. The 510(k) number is K060367.

When did TENOLIG receive FDA 510(k) clearance?

TENOLIG received FDA 510(k) clearance on 2006-08-09, under 510(k) number K060367.

Who is the listed applicant for TENOLIG?

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

What is the FDA product code for TENOLIG?

The FDA product code for TENOLIG is GAT.

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Related Devices (Code: GAT)

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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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