FDA 510(k)

BD RECYKLEEN SHARPS COLLECTORS

K-Number: K112774 · 2012-03-28

Decision Date2012-03-28

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BD RECYKLEEN SHARPS COLLECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2012-03-28 under 510(k) number K112774. 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 BD RECYKLEEN SHARPS COLLECTORS?

BD RECYKLEEN SHARPS COLLECTORS is a medical device that received FDA 510(k) clearance on 2012-03-28. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K112774.

When did BD RECYKLEEN SHARPS COLLECTORS receive FDA 510(k) clearance?

BD RECYKLEEN SHARPS COLLECTORS received FDA 510(k) clearance on 2012-03-28, under 510(k) number K112774.

Who is the listed applicant for BD RECYKLEEN SHARPS COLLECTORS?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD RECYKLEEN SHARPS COLLECTORS?

The FDA product code for BD RECYKLEEN SHARPS COLLECTORS is MMK.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.