DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
K-Number: K001337 · 2000-07-05
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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