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FDA 510(k)

ARM-A-VIAL LV SODIUM CHLORIDE INHALAT

K-Number: K841989 · 1984-07-27

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

Device Summary

ARM-A-VIAL LV SODIUM CHLORIDE INHALAT 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 K841989. 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-VIAL LV SODIUM CHLORIDE INHALAT?

ARM-A-VIAL LV SODIUM CHLORIDE INHALAT 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 K841989.

When did ARM-A-VIAL LV SODIUM CHLORIDE INHALAT receive FDA 510(k) clearance?

ARM-A-VIAL LV SODIUM CHLORIDE INHALAT received FDA 510(k) clearance on 1984-07-27, under 510(k) number K841989.

Who is the listed applicant for ARM-A-VIAL LV SODIUM CHLORIDE INHALAT?

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-VIAL LV SODIUM CHLORIDE INHALAT?

The FDA product code for ARM-A-VIAL LV SODIUM CHLORIDE INHALAT is CCQ.

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Other records listing Armour Pharmaceutical Co. 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.

K842209ARM-A-FLOW INTRAVENOUS FLOW REGULATORK844005ARM-A-VIAL LV HEATER-BREATHING SYSK841991ARM-A-CARE HUMIDIFIER-RESPIRATORY GASK841990ARM-A-CARE NEBULIZER-NEBULIZERK841988ARM-A-VIAL LV SODIUM, CHLORIDE INHALATK841987ARM-A-VIAL LV STERIAL WATER FOR INHALA

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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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