INTRODUCER FOR ENDOTRACHEAL TUBE
K-Number: K820451 · 1982-03-26
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Device Summary
Frequently Asked Questions
What is the INTRODUCER FOR ENDOTRACHEAL TUBE?
INTRODUCER FOR ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1982-03-26. The listed applicant is Imed Corp.. The 510(k) number is K820451.
When did INTRODUCER FOR ENDOTRACHEAL TUBE receive FDA 510(k) clearance?
INTRODUCER FOR ENDOTRACHEAL TUBE received FDA 510(k) clearance on 1982-03-26, under 510(k) number K820451.
Who is the listed applicant for INTRODUCER FOR ENDOTRACHEAL TUBE?
The FDA 510(k) record lists Imed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRODUCER FOR ENDOTRACHEAL TUBE?
The FDA product code for INTRODUCER FOR ENDOTRACHEAL TUBE is BWB.
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 Imed 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: BWB)
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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