FDA 510(k)

SHARPS CONTAINER, MODEL 039-413

K-Number: K063666 · 2007-01-25

Decision Date2007-01-25

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SHARPS CONTAINER, MODEL 039-413 is the device name listed in this FDA 510(k) record. The listed applicant is Biodex Medical Systems, Inc.. It received FDA 510(k) clearance on 2007-01-25 under 510(k) number K063666. 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 CONTAINER, MODEL 039-413?

SHARPS CONTAINER, MODEL 039-413 is a medical device that received FDA 510(k) clearance on 2007-01-25. The listed applicant is Biodex Medical Systems, Inc.. The 510(k) number is K063666.

When did SHARPS CONTAINER, MODEL 039-413 receive FDA 510(k) clearance?

SHARPS CONTAINER, MODEL 039-413 received FDA 510(k) clearance on 2007-01-25, under 510(k) number K063666.

Who is the listed applicant for SHARPS CONTAINER, MODEL 039-413?

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

What is the FDA product code for SHARPS CONTAINER, MODEL 039-413?

The FDA product code for SHARPS CONTAINER, MODEL 039-413 is MMK.

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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.