FDA 510(k)

MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER

K-Number: K943578 · 1994-08-23

Decision Date1994-08-23

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K943578. 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 MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER?

MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Sherwood Medical Co.. The 510(k) number is K943578.

When did MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER receive FDA 510(k) clearance?

MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER received FDA 510(k) clearance on 1994-08-23, under 510(k) number K943578.

Who is the listed applicant for MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER?

The FDA product code for MONOJECT HIGH VOLUME/CHEMOTHERAPY SHARPS CONTAINER is 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.