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FDA 510(k)

SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380

K-Number: K871189 · 1987-05-08

ApplicantSunbeam Appliance Service Co.
Decision Date1987-05-08
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 is the device name listed in this FDA 510(k) record. The listed applicant is Sunbeam Appliance Service Co.. It received FDA 510(k) clearance on 1987-05-08 under 510(k) number K871189. 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 SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380?

SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 is a medical device that received FDA 510(k) clearance on 1987-05-08. The listed applicant is Sunbeam Appliance Service Co.. The 510(k) number is K871189.

When did SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 receive FDA 510(k) clearance?

SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 received FDA 510(k) clearance on 1987-05-08, under 510(k) number K871189.

Who is the listed applicant for SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380?

The FDA 510(k) record lists Sunbeam Appliance Service Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380?

The FDA product code for SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 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.K862919TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIERTranspirator Technologics, Inc.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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