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FDA 510(k)

24 CELL WELLS TISSUE CULTURE

K-Number: K823747 · 1983-01-05

ApplicantCorning Medical & Scientific
Decision Date1983-01-05
Product CodeKJG
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

24 CELL WELLS TISSUE CULTURE is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1983-01-05 under 510(k) number K823747. The device is classified under product code KJG. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 24 CELL WELLS TISSUE CULTURE?

24 CELL WELLS TISSUE CULTURE is a medical device that received FDA 510(k) clearance on 1983-01-05. The listed applicant is Corning Medical & Scientific. The 510(k) number is K823747.

When did 24 CELL WELLS TISSUE CULTURE receive FDA 510(k) clearance?

24 CELL WELLS TISSUE CULTURE received FDA 510(k) clearance on 1983-01-05, under 510(k) number K823747.

Who is the listed applicant for 24 CELL WELLS TISSUE CULTURE?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 24 CELL WELLS TISSUE CULTURE?

The FDA product code for 24 CELL WELLS TISSUE CULTURE is KJG.

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Other records listing Corning Medical & Scientific 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.

K875122DISPOSABLE STERILE SYRINGE FILTERSK872273CORNING EASY WASH ELISA PLATESK872076CORNING DISPOSABLE ROLLER BOTTLESK863789CORNING ELISA PLATESK854024CORNING MAGIC MAB HCG RADIOIMMUNOASSAYK853634CORNING CELL WELLS-MULTIPLE WELL PLATES

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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