FDA 510(k)

BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE

K-Number: K052843 · 2006-04-17

ApplicantBusse Hospital Disposables, Inc.

Decision Date2006-04-17

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hospital Disposables, Inc.. It received FDA 510(k) clearance on 2006-04-17 under 510(k) number K052843. 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 BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE?

BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE is a medical device that received FDA 510(k) clearance on 2006-04-17. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K052843.

When did BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE receive FDA 510(k) clearance?

BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE received FDA 510(k) clearance on 2006-04-17, under 510(k) number K052843.

Who is the listed applicant for BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE?

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

What is the FDA product code for BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE?

The FDA product code for BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE is FMI.

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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.