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FDA 510(k)

MULTIWELL CULTURE PLATE INSERTS

K-Number: K890542 · 1989-02-14

Decision Date1989-02-14
Product CodeKIZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MULTIWELL CULTURE PLATE INSERTS is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1989-02-14 under 510(k) number K890542. The device is classified under product code KIZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIWELL CULTURE PLATE INSERTS?

MULTIWELL CULTURE PLATE INSERTS is a medical device that received FDA 510(k) clearance on 1989-02-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K890542.

When did MULTIWELL CULTURE PLATE INSERTS receive FDA 510(k) clearance?

MULTIWELL CULTURE PLATE INSERTS received FDA 510(k) clearance on 1989-02-14, under 510(k) number K890542.

Who is the listed applicant for MULTIWELL CULTURE PLATE INSERTS?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIWELL CULTURE PLATE INSERTS?

The FDA product code for MULTIWELL CULTURE PLATE INSERTS is KIZ.

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.

Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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.

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Related Devices (Code: KIZ)

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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