SHARPSTANK REUSABLE SHARPS CONTAINER
K-Number: K131087 · 2013-07-12
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Device Summary
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
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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