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FDA 510(k)

AEROCHAMBER W/MASK, MODIFIED

K-Number: K930574 · 1994-01-24

ApplicantMonaghan Medical Corp.
Decision Date1994-01-24
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROCHAMBER W/MASK, MODIFIED 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 1994-01-24 under 510(k) number K930574. 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 AEROCHAMBER W/MASK, MODIFIED?

AEROCHAMBER W/MASK, MODIFIED is a medical device that received FDA 510(k) clearance on 1994-01-24. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K930574.

When did AEROCHAMBER W/MASK, MODIFIED receive FDA 510(k) clearance?

AEROCHAMBER W/MASK, MODIFIED received FDA 510(k) clearance on 1994-01-24, under 510(k) number K930574.

Who is the listed applicant for AEROCHAMBER W/MASK, MODIFIED?

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 AEROCHAMBER W/MASK, MODIFIED?

The FDA product code for AEROCHAMBER W/MASK, MODIFIED is CAF.

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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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