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FDA 510(k)

SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2

K-Number: K091736 · 2009-10-30

Decision Date2009-10-30
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2 is the device name listed in this FDA 510(k) record. The listed applicant is Daniels Corporation Pty, Inc.. It received FDA 510(k) clearance on 2009-10-30 under 510(k) number K091736. 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 SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2?

SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2 is a medical device that received FDA 510(k) clearance on 2009-10-30. The listed applicant is Daniels Corporation Pty, Inc.. The 510(k) number is K091736.

When did SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2 receive FDA 510(k) clearance?

SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2 received FDA 510(k) clearance on 2009-10-30, under 510(k) number K091736.

Who is the listed applicant for SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2?

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

What is the FDA product code for SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2?

The FDA product code for SHARPSMART DISPOSABLE SHARPS CONTAINER, MODEL S2 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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