902 NA/K
K-Number: K811896 · 1981-07-23
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Device Summary
Frequently Asked Questions
What is the 902 NA/K?
902 NA/K is a medical device that received FDA 510(k) clearance on 1981-07-23. The listed applicant is Corning Medical & Scientific. The 510(k) number is K811896.
When did 902 NA/K receive FDA 510(k) clearance?
902 NA/K received FDA 510(k) clearance on 1981-07-23, under 510(k) number K811896.
Who is the listed applicant for 902 NA/K?
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 902 NA/K?
The FDA product code for 902 NA/K is JGS.
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: JGS)
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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