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FDA 510(k)

DANIELS SHARPSMART REUSABLE SHARPS CONTAINER

K-Number: K001337 · 2000-07-05

Decision Date2000-07-05
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DANIELS SHARPSMART REUSABLE SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is The Daniels Corp.. It received FDA 510(k) clearance on 2000-07-05 under 510(k) number K001337. 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 DANIELS SHARPSMART REUSABLE SHARPS CONTAINER?

DANIELS SHARPSMART REUSABLE SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 2000-07-05. The listed applicant is The Daniels Corp.. The 510(k) number is K001337.

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

DANIELS SHARPSMART REUSABLE SHARPS CONTAINER received FDA 510(k) clearance on 2000-07-05, under 510(k) number K001337.

Who is the listed applicant for DANIELS SHARPSMART REUSABLE SHARPS CONTAINER?

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

What is the FDA product code for DANIELS SHARPSMART REUSABLE SHARPS CONTAINER?

The FDA product code for DANIELS SHARPSMART 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.

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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