Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OAK RIDGE PRODUCTS SHARP CONTAINER

K-Number: K130281 · 2013-06-21

Decision Date2013-06-21
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OAK RIDGE PRODUCTS SHARP CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Oak Ridge Products, LLC. It received FDA 510(k) clearance on 2013-06-21 under 510(k) number K130281. 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 OAK RIDGE PRODUCTS SHARP CONTAINER?

OAK RIDGE PRODUCTS SHARP CONTAINER is a medical device that received FDA 510(k) clearance on 2013-06-21. The listed applicant is Oak Ridge Products, LLC. The 510(k) number is K130281.

When did OAK RIDGE PRODUCTS SHARP CONTAINER receive FDA 510(k) clearance?

OAK RIDGE PRODUCTS SHARP CONTAINER received FDA 510(k) clearance on 2013-06-21, under 510(k) number K130281.

Who is the listed applicant for OAK RIDGE PRODUCTS SHARP CONTAINER?

The FDA 510(k) record lists Oak Ridge Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OAK RIDGE PRODUCTS SHARP CONTAINER?

The FDA product code for OAK RIDGE PRODUCTS SHARP 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 Oak Ridge Products, LLC 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.

↑