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FDA 510(k)

PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER

K-Number: K896481 · 1990-05-15

ApplicantPurebrush Assoc.
Decision Date1990-05-15
Product CodeMCF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Purebrush Assoc.. It received FDA 510(k) clearance on 1990-05-15 under 510(k) number K896481. The device is classified under product code MCF. It was reviewed by the DE advisory panel. Product code MCF falls under the category of Surgical Instruments, which includes handheld instruments for general and specialized surgical procedures. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER?

PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Purebrush Assoc.. The 510(k) number is K896481.

When did PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER receive FDA 510(k) clearance?

PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER received FDA 510(k) clearance on 1990-05-15, under 510(k) number K896481.

Who is the listed applicant for PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER?

The FDA 510(k) record lists Purebrush Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER?

The FDA product code for PUREBRUSH ULTRAVIOLET TOOTHBRUSH SANITIZER is MCF. This falls under the Surgical Instruments category.

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

Related Devices (Code: MCF)

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.

K023662PROSONIC ULTRAVIOLET TOOTHBRUSH SANITIZERHwadong International Company , Ltd.K021258GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZERGerm Terminator CorporationK003517OTRES TOOTHBRUSH SANITIZER MODEL TB100WOtres, LLCK901459DS60 TOOTHBRUSH SANITIZERAssociated Mills, 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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