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FDA 510(k)

MICRO-VENT NEBULIZER SYSTEM

K-Number: K904717 · 1991-04-01

Decision Date1991-04-01
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICRO-VENT NEBULIZER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tri/Bor Medical, Inc.. It received FDA 510(k) clearance on 1991-04-01 under 510(k) number K904717. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-VENT NEBULIZER SYSTEM?

MICRO-VENT NEBULIZER SYSTEM is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Tri/Bor Medical, Inc.. The 510(k) number is K904717.

When did MICRO-VENT NEBULIZER SYSTEM receive FDA 510(k) clearance?

MICRO-VENT NEBULIZER SYSTEM received FDA 510(k) clearance on 1991-04-01, under 510(k) number K904717.

Who is the listed applicant for MICRO-VENT NEBULIZER SYSTEM?

The FDA 510(k) record lists Tri/Bor Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-VENT NEBULIZER SYSTEM?

The FDA product code for MICRO-VENT NEBULIZER SYSTEM is CAF.

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 Tri/Bor Medical, 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.

Related Devices (Code: CAF)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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