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FDA 510(k)

MP-500 ELECTRONIC NEBULIZER

K-Number: K862171 · 1986-07-14

ApplicantThe Timeter Group
Decision Date1986-07-14
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MP-500 ELECTRONIC NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is The Timeter Group. It received FDA 510(k) clearance on 1986-07-14 under 510(k) number K862171. The device is classified under product code KFZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MP-500 ELECTRONIC NEBULIZER?

MP-500 ELECTRONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 1986-07-14. The listed applicant is The Timeter Group. The 510(k) number is K862171.

When did MP-500 ELECTRONIC NEBULIZER receive FDA 510(k) clearance?

MP-500 ELECTRONIC NEBULIZER received FDA 510(k) clearance on 1986-07-14, under 510(k) number K862171.

Who is the listed applicant for MP-500 ELECTRONIC NEBULIZER?

The FDA 510(k) record lists The Timeter Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MP-500 ELECTRONIC NEBULIZER?

The FDA product code for MP-500 ELECTRONIC NEBULIZER is KFZ.

Related Clinical Trials

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.

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Other records listing The Timeter Group 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.

K871452CLASSIC (TM) 200 OXYGEN FLOWMETERK852374OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18K844556KHM 2000 DRIP WATCHER

Related Devices (Code: KFZ)

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.

K950116THERASTEAM PERSONAL STEAM INHALERKaz, Inc.K915603VIROTHERM HUMIDIFIERVirotherm LaboratoryK894734RHINOTHERM ULTRA 2Twinmed Products, Inc.K871661WH150 ROOM HUMIDIFIERAssociated Mills, Inc.K871189SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380Sunbeam Appliance Service Co.K862919TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIERTranspirator Technologics, 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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