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FDA 510(k)

TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER

K-Number: K862919 · 1986-11-07

ApplicantTranspirator Technologics, Inc.
Decision Date1986-11-07
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Transpirator Technologics, Inc.. It received FDA 510(k) clearance on 1986-11-07 under 510(k) number K862919. 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 TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER?

TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1986-11-07. The listed applicant is Transpirator Technologics, Inc.. The 510(k) number is K862919.

When did TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER receive FDA 510(k) clearance?

TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER received FDA 510(k) clearance on 1986-11-07, under 510(k) number K862919.

Who is the listed applicant for TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER?

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

What is the FDA product code for TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER?

The FDA product code for TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER is KFZ.

Related Clinical Trials

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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.K862171MP-500 ELECTRONIC NEBULIZERThe Timeter Group

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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