FDA 510(k)

SHARPTRACK REUSABLE SHARPS CONTAINER

K-Number: K981184 · 1998-06-22

Decision Date1998-06-22

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SHARPTRACK REUSABLE SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Bfi- Medical Waste Systems. It received FDA 510(k) clearance on 1998-06-22 under 510(k) number K981184. 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 SHARPTRACK REUSABLE SHARPS CONTAINER?

SHARPTRACK REUSABLE SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 1998-06-22. The listed applicant is Bfi- Medical Waste Systems. The 510(k) number is K981184.

When did SHARPTRACK REUSABLE SHARPS CONTAINER receive FDA 510(k) clearance?

SHARPTRACK REUSABLE SHARPS CONTAINER received FDA 510(k) clearance on 1998-06-22, under 510(k) number K981184.

Who is the listed applicant for SHARPTRACK REUSABLE SHARPS CONTAINER?

The FDA 510(k) record lists Bfi- Medical Waste Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARPTRACK REUSABLE SHARPS CONTAINER?

The FDA product code for SHARPTRACK REUSABLE SHARPS CONTAINER is FMI.

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Other records listing Bfi- Medical Waste Systems as applicant

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Related Devices (Code: FMI)

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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.