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FDA 510(k)

SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664

K-Number: K851220 · 1985-09-17

Decision Date1985-09-17
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 is the device name listed in this FDA 510(k) record. The listed applicant is Northern Electric Co. Div. of Sunbeam Corp.. It received FDA 510(k) clearance on 1985-09-17 under 510(k) number K851220. 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 EVAPORATIVE HUMIDIFIER 663 & 664?

SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 is a medical device that received FDA 510(k) clearance on 1985-09-17. The listed applicant is Northern Electric Co. Div. of Sunbeam Corp.. The 510(k) number is K851220.

When did SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 receive FDA 510(k) clearance?

SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 received FDA 510(k) clearance on 1985-09-17, under 510(k) number K851220.

Who is the listed applicant for SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664?

The FDA 510(k) record lists Northern Electric Co. Div. of Sunbeam Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664?

The FDA product code for SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 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.

Other records listing Northern Electric Co. Div. of Sunbeam Corp. 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.

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.

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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