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FDA 510(k)

SHARPSTANK REUSABLE SHARPS CONTAINER

K-Number: K131087 · 2013-07-12

Decision Date2013-07-12
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPSTANK REUSABLE SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Rehrig Pacific Company. It received FDA 510(k) clearance on 2013-07-12 under 510(k) number K131087. 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 SHARPSTANK REUSABLE SHARPS CONTAINER?

SHARPSTANK REUSABLE SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 2013-07-12. The listed applicant is Rehrig Pacific Company. The 510(k) number is K131087.

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

SHARPSTANK REUSABLE SHARPS CONTAINER received FDA 510(k) clearance on 2013-07-12, under 510(k) number K131087.

Who is the listed applicant for SHARPSTANK REUSABLE SHARPS CONTAINER?

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

What is the FDA product code for SHARPSTANK REUSABLE SHARPS CONTAINER?

The FDA product code for SHARPSTANK REUSABLE SHARPS 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 Rehrig Pacific Company 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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