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FDA 510(k)

SEKURIT SHARPS COLLECTION CONTAINER

K-Number: K063722 · 2007-03-05

Decision Date2007-03-05
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEKURIT SHARPS COLLECTION CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Techen Safety, Inc.. It received FDA 510(k) clearance on 2007-03-05 under 510(k) number K063722. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEKURIT SHARPS COLLECTION CONTAINER?

SEKURIT SHARPS COLLECTION CONTAINER is a medical device that received FDA 510(k) clearance on 2007-03-05. The listed applicant is Techen Safety, Inc.. The 510(k) number is K063722.

When did SEKURIT SHARPS COLLECTION CONTAINER receive FDA 510(k) clearance?

SEKURIT SHARPS COLLECTION CONTAINER received FDA 510(k) clearance on 2007-03-05, under 510(k) number K063722.

Who is the listed applicant for SEKURIT SHARPS COLLECTION CONTAINER?

The FDA 510(k) record lists Techen Safety, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEKURIT SHARPS COLLECTION CONTAINER?

The FDA product code for SEKURIT SHARPS COLLECTION CONTAINER is MMK.

Related Clinical Trials

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.

Related Devices (Code: MMK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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