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FDA 510(k)

APT TRACHEA TUBES

K-Number: K896181 · 1990-01-09

Decision Date1990-01-09
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

APT TRACHEA TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Pulmonary Technologies, Inc.. It received FDA 510(k) clearance on 1990-01-09 under 510(k) number K896181. 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 APT TRACHEA TUBES?

APT TRACHEA TUBES is a medical device that received FDA 510(k) clearance on 1990-01-09. The listed applicant is Advanced Pulmonary Technologies, Inc.. The 510(k) number is K896181.

When did APT TRACHEA TUBES receive FDA 510(k) clearance?

APT TRACHEA TUBES received FDA 510(k) clearance on 1990-01-09, under 510(k) number K896181.

Who is the listed applicant for APT TRACHEA TUBES?

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

What is the FDA product code for APT TRACHEA TUBES?

The FDA product code for APT TRACHEA TUBES 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.

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

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