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FDA 510(k)

MISER INHALATION DEVICE, PART NO. 700

K-Number: K800763 · 1980-04-24

ApplicantVix Breathing Equipment Co.
Decision Date1980-04-24
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MISER INHALATION DEVICE, PART NO. 700 is the device name listed in this FDA 510(k) record. The listed applicant is Vix Breathing Equipment Co.. It received FDA 510(k) clearance on 1980-04-24 under 510(k) number K800763. 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 MISER INHALATION DEVICE, PART NO. 700?

MISER INHALATION DEVICE, PART NO. 700 is a medical device that received FDA 510(k) clearance on 1980-04-24. The listed applicant is Vix Breathing Equipment Co.. The 510(k) number is K800763.

When did MISER INHALATION DEVICE, PART NO. 700 receive FDA 510(k) clearance?

MISER INHALATION DEVICE, PART NO. 700 received FDA 510(k) clearance on 1980-04-24, under 510(k) number K800763.

Who is the listed applicant for MISER INHALATION DEVICE, PART NO. 700?

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

What is the FDA product code for MISER INHALATION DEVICE, PART NO. 700?

The FDA product code for MISER INHALATION DEVICE, PART NO. 700 is CCQ.

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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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