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FDA 510(k)

SHARPS COMPLIANCE CONTAINER

K-Number: K083129 · 2008-12-15

Decision Date2008-12-15
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS COMPLIANCE CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Sharps Compliance, Inc.. It received FDA 510(k) clearance on 2008-12-15 under 510(k) number K083129. 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 COMPLIANCE CONTAINER?

SHARPS COMPLIANCE CONTAINER is a medical device that received FDA 510(k) clearance on 2008-12-15. The listed applicant is Sharps Compliance, Inc.. The 510(k) number is K083129.

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

SHARPS COMPLIANCE CONTAINER received FDA 510(k) clearance on 2008-12-15, under 510(k) number K083129.

Who is the listed applicant for SHARPS COMPLIANCE CONTAINER?

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

What is the FDA product code for SHARPS COMPLIANCE CONTAINER?

The FDA product code for SHARPS COMPLIANCE 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.

Other records listing Sharps Compliance, Inc. 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.

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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