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FDA 510(k)

AVA-NEB NEBULIZER

K-Number: K843102 · 1984-08-17

ApplicantAvatron, Inc.
Decision Date1984-08-17
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AVA-NEB NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Avatron, Inc.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K843102. 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 AVA-NEB NEBULIZER?

AVA-NEB NEBULIZER is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Avatron, Inc.. The 510(k) number is K843102.

When did AVA-NEB NEBULIZER receive FDA 510(k) clearance?

AVA-NEB NEBULIZER received FDA 510(k) clearance on 1984-08-17, under 510(k) number K843102.

Who is the listed applicant for AVA-NEB NEBULIZER?

The FDA 510(k) record lists Avatron, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVA-NEB NEBULIZER?

The FDA product code for AVA-NEB NEBULIZER is CCQ.

Related Clinical Trials

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Other records listing Avatron, Inc. 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.

K851193ANESTHESIA BREATHING CIRCUITK844956AVA-MIST PORTABLE AIR COMPRESSORK842778AVATRON UNIVERSAL ADULT VOL. VENTILATORK842389AVATRON DISPOSABLE I.P.P.B. CIRUCIT

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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