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FDA 510(k)

THE SHARPS COLLECTION AND DISPOSAL SYSTEM

K-Number: K945197 · 1994-12-02

Decision Date1994-12-02
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE SHARPS COLLECTION AND DISPOSAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1994-12-02 under 510(k) number K945197. 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 THE SHARPS COLLECTION AND DISPOSAL SYSTEM?

THE SHARPS COLLECTION AND DISPOSAL SYSTEM is a medical device that received FDA 510(k) clearance on 1994-12-02. The listed applicant is Devon Industries, Inc.. The 510(k) number is K945197.

When did THE SHARPS COLLECTION AND DISPOSAL SYSTEM receive FDA 510(k) clearance?

THE SHARPS COLLECTION AND DISPOSAL SYSTEM received FDA 510(k) clearance on 1994-12-02, under 510(k) number K945197.

Who is the listed applicant for THE SHARPS COLLECTION AND DISPOSAL SYSTEM?

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

What is the FDA product code for THE SHARPS COLLECTION AND DISPOSAL SYSTEM?

The FDA product code for THE SHARPS COLLECTION AND DISPOSAL SYSTEM 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 Devon Industries, Inc. 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.

View all 47 devices →

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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