Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NO-MES

K-Number: K935633 · 1994-09-30

ApplicantEthox Corp.
Decision Date1994-09-30
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NO-MES is the device name listed in this FDA 510(k) record. The listed applicant is Ethox Corp.. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K935633. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 19 devices →

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.

↑