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FDA 510(k)

ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO

K-Number: K926301 · 1993-07-21

ApplicantDhd Diemolding Healthcare Div.
Decision Date1993-07-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Diemolding Healthcare Div.. It received FDA 510(k) clearance on 1993-07-21 under 510(k) number K926301. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO?

ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO is a medical device that received FDA 510(k) clearance on 1993-07-21. The listed applicant is Dhd Diemolding Healthcare Div.. The 510(k) number is K926301.

When did ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO receive FDA 510(k) clearance?

ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO received FDA 510(k) clearance on 1993-07-21, under 510(k) number K926301.

Who is the listed applicant for ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO?

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

What is the FDA product code for ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO?

The FDA product code for ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO is CAF.

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Other records listing Dhd Diemolding Healthcare Div. 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.

K973532STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATORK970596DHD EMERALD PRODUCTK961973DHD ACE WITH MASK KITK953206DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)K945118EXPIRATORY BREATHING EXERCISERK944900THERAPEP

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Related Devices (Code: CAF)

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.

K254171Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebulizer (UN209); Mesh Nebulizer (UN210)Shenzhen Mericonn Technology Co., Ltd.K260270FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)FindAir Sp. z o.o.K251572eRapid with eTrack SystemPari Respiratory Equipment, Inc.K251659Mesh Nebulizer (H6)Qingdao Future Medical Technology Co., Ltd.K244035Portable mesh nebulizer (JM821)Shenzhen Jermei Medical Device Technology Co., Ltd.K243468Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer (NB-1102); Compressor Nebulizer (NB-1103)Joytech Healthcare Co. , Ltd.

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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