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FDA 510(k)

MICRO BRIGHT VENTILATION TUBES

K-Number: K903285 · 1990-09-26

Decision Date1990-09-26
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICRO BRIGHT VENTILATION TUBES 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 1990-09-26 under 510(k) number K903285. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO BRIGHT VENTILATION TUBES?

MICRO BRIGHT VENTILATION TUBES is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Invotec International, Inc.. The 510(k) number is K903285.

When did MICRO BRIGHT VENTILATION TUBES receive FDA 510(k) clearance?

MICRO BRIGHT VENTILATION TUBES received FDA 510(k) clearance on 1990-09-26, under 510(k) number K903285.

Who is the listed applicant for MICRO BRIGHT VENTILATION TUBES?

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 MICRO BRIGHT VENTILATION TUBES?

The FDA product code for MICRO BRIGHT VENTILATION TUBES is ETD.

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: ETD)

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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