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FDA 510(k)

MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER

K-Number: K900557 · 1991-04-10

ApplicantMonaghan Medical Corp.
Decision Date1991-04-10
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER 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 1991-04-10 under 510(k) number K900557. 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 MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER?

MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER is a medical device that received FDA 510(k) clearance on 1991-04-10. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K900557.

When did MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER receive FDA 510(k) clearance?

MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER received FDA 510(k) clearance on 1991-04-10, under 510(k) number K900557.

Who is the listed applicant for MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER?

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 MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER?

The FDA product code for MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER is CCQ.

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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.

K123945STRIVE DUAL ZONE PEAK FLOW METERK031514MODIFICATION TO TRUPEAK PEAK FLOW METERK023097TRUEZONE PEAK FLOW METERK012939AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBERK991212MODIFICATION TO TRUZONE PEAK FLOW METERK964130AEROGEAR ASTHMA ACTION KIT

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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.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, Inc.

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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