Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220

K-Number: K860118 · 1986-04-17

ApplicantNorthern Electric Co. Div. of Sunbeam Corp.
Decision Date1986-04-17
Product CodeEFT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220 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 1986-04-17 under 510(k) number K860118. The device is classified under product code EFT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220?

SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220 is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Northern Electric Co. Div. of Sunbeam Corp.. The 510(k) number is K860118.

When did SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220 receive FDA 510(k) clearance?

SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220 received FDA 510(k) clearance on 1986-04-17, under 510(k) number K860118.

Who is the listed applicant for SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220?

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 ULTRASONIC DENTURE CLEANER MODEL 4220?

The FDA product code for SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220 is EFT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K851220SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664K852593SUNBEAM DENTAL CARE CENTER, MODEL NO. 6273K852279SUNBEAM RECHARGEABLE TOOTHBRUSH MODEL # 4201

Related Devices (Code: EFT)

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.

K080631CLEANSE.FRESHEN.GO; ALIGNER CLEANSING TOWELETTE AND DENTAL APPLIANCE CLEANSEROral Health Technologies, LLCK051342MEDICAL INTERPOROUSBonyf AGK000996TRUBYTE DENTURE CLEANSER/POLISHING COMPOUNDDentsply Intl.K942203OTC DENTURE CLEANSERCombe, Inc.K930337PROFAST(R)-DENTURE CLEANSERFittydent-Altwirth & Schmitt GmbHK914257DENTURE PRODUCT XEssential Dental Systems, 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.

↑