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FDA 510(k)

SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE

K-Number: K944738 · 1994-10-19

ApplicantDucker CL
Decision Date1994-10-19
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE is the device name listed in this FDA 510(k) record. The listed applicant is Ducker CL. It received FDA 510(k) clearance on 1994-10-19 under 510(k) number K944738. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE?

SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1994-10-19. The listed applicant is Ducker CL. The 510(k) number is K944738.

When did SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE receive FDA 510(k) clearance?

SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE received FDA 510(k) clearance on 1994-10-19, under 510(k) number K944738.

Who is the listed applicant for SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE?

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

What is the FDA product code for SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE?

The FDA product code for SERIES 600 CENTRIFUGE-FOUR SEPARATE VARIATIONS OF THE SAME BASE CENTRIFUGE is JQC.

Related Clinical Trials

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.

Related Devices (Code: JQC)

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.

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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