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FDA 510(k)

ULTRASONIC HUMIDIFIER

K-Number: K790966 · 1979-06-11

ApplicantHankscraft Div. of Gerber Products Co.
Decision Date1979-06-11
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Hankscraft Div. of Gerber Products Co.. It received FDA 510(k) clearance on 1979-06-11 under 510(k) number K790966. 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 ULTRASONIC HUMIDIFIER?

ULTRASONIC HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1979-06-11. The listed applicant is Hankscraft Div. of Gerber Products Co.. The 510(k) number is K790966.

When did ULTRASONIC HUMIDIFIER receive FDA 510(k) clearance?

ULTRASONIC HUMIDIFIER received FDA 510(k) clearance on 1979-06-11, under 510(k) number K790966.

Who is the listed applicant for ULTRASONIC HUMIDIFIER?

The FDA 510(k) record lists Hankscraft Div. of Gerber Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASONIC HUMIDIFIER?

The FDA product code for ULTRASONIC HUMIDIFIER 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 Hankscraft Div. of Gerber Products Co. 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.

K844013CARE ELECTRIC BREAST PUMP

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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