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FDA 510(k)

MULTI-CENTRIFUGE

K-Number: K955795 · 1996-03-29

ApplicantNovonx, Inc.
Decision Date1996-03-29
Product CodeGKG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MULTI-CENTRIFUGE is the device name listed in this FDA 510(k) record. The listed applicant is Novonx, Inc.. It received FDA 510(k) clearance on 1996-03-29 under 510(k) number K955795. The device is classified under product code GKG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-CENTRIFUGE?

MULTI-CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is Novonx, Inc.. The 510(k) number is K955795.

When did MULTI-CENTRIFUGE receive FDA 510(k) clearance?

MULTI-CENTRIFUGE received FDA 510(k) clearance on 1996-03-29, under 510(k) number K955795.

Who is the listed applicant for MULTI-CENTRIFUGE?

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

What is the FDA product code for MULTI-CENTRIFUGE?

The FDA product code for MULTI-CENTRIFUGE is GKG.

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Related Devices (Code: GKG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K961803SPUNCRIT (MODEL DRC-40)Micro Diagnostics Corp.K930415MICROHEMATOCRIT ROTORFisher Scientific Co., LLCK925863SPUNCRITbioMerieux, Inc.K920207HERMLE Z230HLabnet Intl., Inc.K920759CRITSPIN MICRO-HEMATOCRITStat-Spin TechnologiesK913128HEMATASTAT C-70BSeparation Technology, Inc.

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.

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