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FDA 510(k)

AMSINO ENDOTRACHEAL TUBE

K-Number: K050785 · 2005-07-15

Decision Date2005-07-15
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AMSINO ENDOTRACHEAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Amsino International, Inc.. It received FDA 510(k) clearance on 2005-07-15 under 510(k) number K050785. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSINO ENDOTRACHEAL TUBE?

AMSINO ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 2005-07-15. The listed applicant is Amsino International, Inc.. The 510(k) number is K050785.

When did AMSINO ENDOTRACHEAL TUBE receive FDA 510(k) clearance?

AMSINO ENDOTRACHEAL TUBE received FDA 510(k) clearance on 2005-07-15, under 510(k) number K050785.

Who is the listed applicant for AMSINO ENDOTRACHEAL TUBE?

The FDA 510(k) record lists Amsino International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSINO ENDOTRACHEAL TUBE?

The FDA product code for AMSINO ENDOTRACHEAL TUBE is BTR.

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 Amsino International, Inc. 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 28 devices →

Related Devices (Code: BTR)

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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