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FDA 510(k)

SHARPS SAFE 1.5 & SHARPS SAFE 2.0

K-Number: K955514 · 1996-08-01

Decision Date1996-08-01
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS SAFE 1.5 & SHARPS SAFE 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Dura-Vac Products. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K955514. 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 SHARPS SAFE 1.5 & SHARPS SAFE 2.0?

SHARPS SAFE 1.5 & SHARPS SAFE 2.0 is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Dura-Vac Products. The 510(k) number is K955514.

When did SHARPS SAFE 1.5 & SHARPS SAFE 2.0 receive FDA 510(k) clearance?

SHARPS SAFE 1.5 & SHARPS SAFE 2.0 received FDA 510(k) clearance on 1996-08-01, under 510(k) number K955514.

Who is the listed applicant for SHARPS SAFE 1.5 & SHARPS SAFE 2.0?

The FDA 510(k) record lists Dura-Vac Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARPS SAFE 1.5 & SHARPS SAFE 2.0?

The FDA product code for SHARPS SAFE 1.5 & SHARPS SAFE 2.0 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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