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FDA 510(k)

TRACHEOSTOMY T-TUBE

K-Number: K930114 · 1993-03-19

Decision Date1993-03-19
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRACHEOSTOMY T-TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Invotec International, Inc.. It received FDA 510(k) clearance on 1993-03-19 under 510(k) number K930114. 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 TRACHEOSTOMY T-TUBE?

TRACHEOSTOMY T-TUBE is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Invotec International, Inc.. The 510(k) number is K930114.

When did TRACHEOSTOMY T-TUBE receive FDA 510(k) clearance?

TRACHEOSTOMY T-TUBE received FDA 510(k) clearance on 1993-03-19, under 510(k) number K930114.

Who is the listed applicant for TRACHEOSTOMY T-TUBE?

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

What is the FDA product code for TRACHEOSTOMY T-TUBE?

The FDA product code for TRACHEOSTOMY T-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 Invotec 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 16 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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