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FDA 510(k)

ARM-A-CARE NEBULIZER-NEBULIZER

K-Number: K841990 · 1984-07-27

ApplicantArmour Pharmaceutical Co.
Decision Date1984-07-27
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARM-A-CARE NEBULIZER-NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Armour Pharmaceutical Co.. It received FDA 510(k) clearance on 1984-07-27 under 510(k) number K841990. 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 ARM-A-CARE NEBULIZER-NEBULIZER?

ARM-A-CARE NEBULIZER-NEBULIZER is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Armour Pharmaceutical Co.. The 510(k) number is K841990.

When did ARM-A-CARE NEBULIZER-NEBULIZER receive FDA 510(k) clearance?

ARM-A-CARE NEBULIZER-NEBULIZER received FDA 510(k) clearance on 1984-07-27, under 510(k) number K841990.

Who is the listed applicant for ARM-A-CARE NEBULIZER-NEBULIZER?

The FDA 510(k) record lists Armour Pharmaceutical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARM-A-CARE NEBULIZER-NEBULIZER?

The FDA product code for ARM-A-CARE NEBULIZER-NEBULIZER is CCQ.

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Other records listing Armour Pharmaceutical Co. as applicant

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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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