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FDA 510(k)

THE CEN-SLIDE(TM) CENTRIFUGE TUBE

K-Number: K891604 · 1989-06-16

Decision Date1989-06-16
Product CodeKEW
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

THE CEN-SLIDE(TM) CENTRIFUGE TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Davstar California, Inc.. It received FDA 510(k) clearance on 1989-06-16 under 510(k) number K891604. The device is classified under product code KEW. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE CEN-SLIDE(TM) CENTRIFUGE TUBE?

THE CEN-SLIDE(TM) CENTRIFUGE TUBE is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is Davstar California, Inc.. The 510(k) number is K891604.

When did THE CEN-SLIDE(TM) CENTRIFUGE TUBE receive FDA 510(k) clearance?

THE CEN-SLIDE(TM) CENTRIFUGE TUBE received FDA 510(k) clearance on 1989-06-16, under 510(k) number K891604.

Who is the listed applicant for THE CEN-SLIDE(TM) CENTRIFUGE TUBE?

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

What is the FDA product code for THE CEN-SLIDE(TM) CENTRIFUGE TUBE?

The FDA product code for THE CEN-SLIDE(TM) CENTRIFUGE TUBE is KEW.

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: KEW)

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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