ETHOX LAVAGE TUBE
K-Number: K860599 · 1986-03-11
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Device Summary
Frequently Asked Questions
What is the ETHOX LAVAGE TUBE?
ETHOX LAVAGE TUBE is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Ethox Corp.. The 510(k) number is K860599.
When did ETHOX LAVAGE TUBE receive FDA 510(k) clearance?
ETHOX LAVAGE TUBE received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860599.
Who is the listed applicant for ETHOX LAVAGE TUBE?
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 ETHOX LAVAGE TUBE?
The FDA product code for ETHOX LAVAGE TUBE is KDH.
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 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: KDH)
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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