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FDA 510(k)

AEROVENT

K-Number: K894969 · 1989-10-30

Decision Date1989-10-30
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROVENT is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1989-10-30 under 510(k) number K894969. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROVENT?

AEROVENT is a medical device that received FDA 510(k) clearance on 1989-10-30. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K894969.

When did AEROVENT receive FDA 510(k) clearance?

AEROVENT received FDA 510(k) clearance on 1989-10-30, under 510(k) number K894969.

Who is the listed applicant for AEROVENT?

The FDA 510(k) record lists Monaghan Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AEROVENT?

The FDA product code for AEROVENT is BZA.

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 Monaghan Medical Corp. 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 33 devices →

Related Devices (Code: BZA)

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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