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FDA 510(k)

NEBULIZERS

K-Number: K810343 · 1981-03-17

ApplicantTodd Industries, Inc.
Decision Date1981-03-17
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZERS is the device name listed in this FDA 510(k) record. The listed applicant is Todd Industries, Inc.. It received FDA 510(k) clearance on 1981-03-17 under 510(k) number K810343. 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 NEBULIZERS?

NEBULIZERS is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Todd Industries, Inc.. The 510(k) number is K810343.

When did NEBULIZERS receive FDA 510(k) clearance?

NEBULIZERS received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810343.

Who is the listed applicant for NEBULIZERS?

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

What is the FDA product code for NEBULIZERS?

The FDA product code for NEBULIZERS is CCQ.

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Other records listing Todd Industries, 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.

K810340ADULT MASKS & PEDIATRIC MASKSK810341LIFELINE IPPB SET-UPK810362CORRUGATED FLEX TUBINGK810339NOSECLIP #6118K810361CONNECTOR ADAPTERSK810342NASAL CANNULA

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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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