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FDA 510(k)

SHARPS AWAY DISPOSABLE CONTAINER

K-Number: K072667 · 2007-10-10

Decision Date2007-10-10
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS AWAY DISPOSABLE CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Solutions, Inc.. It received FDA 510(k) clearance on 2007-10-10 under 510(k) number K072667. 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 SHARPS AWAY DISPOSABLE CONTAINER?

SHARPS AWAY DISPOSABLE CONTAINER is a medical device that received FDA 510(k) clearance on 2007-10-10. The listed applicant is Solutions, Inc.. The 510(k) number is K072667.

When did SHARPS AWAY DISPOSABLE CONTAINER receive FDA 510(k) clearance?

SHARPS AWAY DISPOSABLE CONTAINER received FDA 510(k) clearance on 2007-10-10, under 510(k) number K072667.

Who is the listed applicant for SHARPS AWAY DISPOSABLE CONTAINER?

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

What is the FDA product code for SHARPS AWAY DISPOSABLE CONTAINER?

The FDA product code for SHARPS AWAY DISPOSABLE 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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