NO-MES
K-Number: K935633 · 1994-09-30
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Device Summary
Frequently Asked Questions
What is the NO-MES?
NO-MES is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Ethox Corp.. The 510(k) number is K935633.
When did NO-MES receive FDA 510(k) clearance?
NO-MES received FDA 510(k) clearance on 1994-09-30, under 510(k) number K935633.
Who is the listed applicant for NO-MES?
The FDA 510(k) record lists Ethox Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NO-MES?
The FDA product code for NO-MES is KNT.
Other records listing Ethox Corp. 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: KNT)
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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