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FDA 510(k)

CIRRUS DRUG NEBULIZER MK III

K-Number: K860875 · 1986-03-20

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1986-03-20
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRRUS DRUG NEBULIZER MK III is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1986-03-20 under 510(k) number K860875. 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 CIRRUS DRUG NEBULIZER MK III?

CIRRUS DRUG NEBULIZER MK III is a medical device that received FDA 510(k) clearance on 1986-03-20. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K860875.

When did CIRRUS DRUG NEBULIZER MK III receive FDA 510(k) clearance?

CIRRUS DRUG NEBULIZER MK III received FDA 510(k) clearance on 1986-03-20, under 510(k) number K860875.

Who is the listed applicant for CIRRUS DRUG NEBULIZER MK III?

The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIRRUS DRUG NEBULIZER MK III?

The FDA product code for CIRRUS DRUG NEBULIZER MK III is CCQ.

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Other records listing Dhd Medical Products Div. Diemolding Corp. 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.

K883988NON-REBREATHING TEE PIECE (NRTP)K881935MICROCIRRUS MEDICAL NEBULIZERK881178CUFFCHECKK873498INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBINGK874047ASTHMAKITK873447DISPOSABLE CONDENSATE BOTTLE FOR 7200 VENTILATOR

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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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