CORNING CELL WELLS-MULTIPLE WELL PLATES
K-Number: K853634 · 1985-09-16
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Device Summary
Frequently Asked Questions
What is the CORNING CELL WELLS-MULTIPLE WELL PLATES?
CORNING CELL WELLS-MULTIPLE WELL PLATES is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Corning Medical & Scientific. The 510(k) number is K853634.
When did CORNING CELL WELLS-MULTIPLE WELL PLATES receive FDA 510(k) clearance?
CORNING CELL WELLS-MULTIPLE WELL PLATES received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853634.
Who is the listed applicant for CORNING CELL WELLS-MULTIPLE WELL PLATES?
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 CORNING CELL WELLS-MULTIPLE WELL PLATES?
The FDA product code for CORNING CELL WELLS-MULTIPLE WELL PLATES 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 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.
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
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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