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FDA 510(k)

DISPO-MED 7.6 LITER SHARPS CONTAINER

K-Number: K003521 · 2001-04-19

Decision Date2001-04-19
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPO-MED 7.6 LITER SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Master Benefits, Inc.. It received FDA 510(k) clearance on 2001-04-19 under 510(k) number K003521. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPO-MED 7.6 LITER SHARPS CONTAINER?

DISPO-MED 7.6 LITER SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 2001-04-19. The listed applicant is Master Benefits, Inc.. The 510(k) number is K003521.

When did DISPO-MED 7.6 LITER SHARPS CONTAINER receive FDA 510(k) clearance?

DISPO-MED 7.6 LITER SHARPS CONTAINER received FDA 510(k) clearance on 2001-04-19, under 510(k) number K003521.

Who is the listed applicant for DISPO-MED 7.6 LITER SHARPS CONTAINER?

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

What is the FDA product code for DISPO-MED 7.6 LITER SHARPS CONTAINER?

The FDA product code for DISPO-MED 7.6 LITER SHARPS CONTAINER is FMI.

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: FMI)

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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