FDA 510(k)

CENTURION KLEEN-NEEDLE SYSTEM

K-Number: K896320 · 1990-01-11

ApplicantTri-State Hospital Supply Corp.

Decision Date1990-01-11

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CENTURION KLEEN-NEEDLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tri-State Hospital Supply Corp.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K896320. 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 CENTURION KLEEN-NEEDLE SYSTEM?

CENTURION KLEEN-NEEDLE SYSTEM is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Tri-State Hospital Supply Corp.. The 510(k) number is K896320.

When did CENTURION KLEEN-NEEDLE SYSTEM receive FDA 510(k) clearance?

CENTURION KLEEN-NEEDLE SYSTEM received FDA 510(k) clearance on 1990-01-11, under 510(k) number K896320.

Who is the listed applicant for CENTURION KLEEN-NEEDLE SYSTEM?

The FDA 510(k) record lists Tri-State Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTURION KLEEN-NEEDLE SYSTEM?

The FDA product code for CENTURION KLEEN-NEEDLE SYSTEM is FMI.

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Other records listing Tri-State Hospital Supply Corp. as applicant

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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.