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FDA 510(k)

RHINOTHERM

K-Number: K840118 · 1984-04-13

ApplicantAscot Pharmaceuticals, Inc.
Decision Date1984-04-13
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RHINOTHERM is the device name listed in this FDA 510(k) record. The listed applicant is Ascot Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840118. 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 RHINOTHERM?

RHINOTHERM is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Ascot Pharmaceuticals, Inc.. The 510(k) number is K840118.

When did RHINOTHERM receive FDA 510(k) clearance?

RHINOTHERM received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840118.

Who is the listed applicant for RHINOTHERM?

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

What is the FDA product code for RHINOTHERM?

The FDA product code for RHINOTHERM is KFZ.

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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.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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