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FDA 510(k)

NEBULIZER HEATER

K-Number: K882935 · 1988-12-27

ApplicantAutomatic Liquid Packaging, Inc.
Decision Date1988-12-27
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER HEATER is the device name listed in this FDA 510(k) record. The listed applicant is Automatic Liquid Packaging, Inc.. It received FDA 510(k) clearance on 1988-12-27 under 510(k) number K882935. 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 NEBULIZER HEATER?

NEBULIZER HEATER is a medical device that received FDA 510(k) clearance on 1988-12-27. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K882935.

When did NEBULIZER HEATER receive FDA 510(k) clearance?

NEBULIZER HEATER received FDA 510(k) clearance on 1988-12-27, under 510(k) number K882935.

Who is the listed applicant for NEBULIZER HEATER?

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

What is the FDA product code for NEBULIZER HEATER?

The FDA product code for NEBULIZER HEATER is CAF.

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Other records listing Automatic Liquid Packaging, 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.

K994321STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USPK000964STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109K980147YOUR CHOICE MULTI-PURPOSE CONTACT LENS CLEANING SOLUTIONK973829IRRIGATION BOTTLEK962079HUMIDIFIER ADAPTERK955104HIGH FLOW ADJUSTABLE ENTRAINMENT NEBULIZER

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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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