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FDA PMA

Sharps needle destruction device

PMA Number: P120018 · 2018-02-16

Decision Date2018-02-16
PMA NumberP120018
Product CodeMTV
Device ClassClass 2
Medical SpecialtyG
Regulation Number21 CFR 8
Advisory CommitteeHO

Device Summary

Sharps needle destruction device is the device name listed in this FDA 510(k) record. The listed applicant is Sharps Terminator, LLC. It received FDA 510(k) clearance on 2018-02-16. The device is classified under product code MTV. It was reviewed by the HO advisory panel.

Frequently Asked Questions

What is the Sharps needle destruction device?

Sharps needle destruction device is a medical device that received FDA 510(k) clearance on 2018-02-16. The listed applicant is Sharps Terminator, LLC.

When did Sharps needle destruction device receive FDA 510(k) clearance?

The clearance date for Sharps needle destruction device can be found in the official FDA records.

Who is the listed applicant for Sharps needle destruction device?

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

What is the FDA product code for Sharps needle destruction device?

The FDA product code for Sharps needle destruction device is MTV.

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 PubMed Literature

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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