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FDA 510(k)

MDI ADAPTOR

K-Number: K900783 · 1990-07-18

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1990-07-18
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MDI ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1990-07-18 under 510(k) number K900783. 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 MDI ADAPTOR?

MDI ADAPTOR is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K900783.

When did MDI ADAPTOR receive FDA 510(k) clearance?

MDI ADAPTOR received FDA 510(k) clearance on 1990-07-18, under 510(k) number K900783.

Who is the listed applicant for MDI ADAPTOR?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDI ADAPTOR?

The FDA product code for MDI ADAPTOR is CAF.

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Other records listing Hudson Oxygen Therapy Sales Co. as applicant

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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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