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FDA 510(k)

MONAGHAN AEROCHAMBER WITH MASK

K-Number: K874513 · 1987-12-30

Decision Date1987-12-30
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONAGHAN AEROCHAMBER WITH MASK 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 1987-12-30 under 510(k) number K874513. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONAGHAN AEROCHAMBER WITH MASK?

MONAGHAN AEROCHAMBER WITH MASK is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K874513.

When did MONAGHAN AEROCHAMBER WITH MASK receive FDA 510(k) clearance?

MONAGHAN AEROCHAMBER WITH MASK received FDA 510(k) clearance on 1987-12-30, under 510(k) number K874513.

Who is the listed applicant for MONAGHAN AEROCHAMBER WITH MASK?

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 MONAGHAN AEROCHAMBER WITH MASK?

The FDA product code for MONAGHAN AEROCHAMBER WITH MASK is CCQ.

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: CCQ)

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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