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FDA 510(k)

MODIFICATION TO:SPECIALTY NEEDLES

K-Number: K073222 · 2008-04-09

ApplicantBusse Hospital Disposables, Inc.
Decision Date2008-04-09
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO:SPECIALTY NEEDLES 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 2008-04-09 under 510(k) number K073222. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO:SPECIALTY NEEDLES?

MODIFICATION TO:SPECIALTY NEEDLES is a medical device that received FDA 510(k) clearance on 2008-04-09. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K073222.

When did MODIFICATION TO:SPECIALTY NEEDLES receive FDA 510(k) clearance?

MODIFICATION TO:SPECIALTY NEEDLES received FDA 510(k) clearance on 2008-04-09, under 510(k) number K073222.

Who is the listed applicant for MODIFICATION TO:SPECIALTY NEEDLES?

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 MODIFICATION TO:SPECIALTY NEEDLES?

The FDA product code for MODIFICATION TO:SPECIALTY NEEDLES is BSP.

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Other records listing Busse Hospital Disposables, Inc. as applicant

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Related Devices (Code: BSP)

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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.

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