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FDA 510(k)

GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER

K-Number: K021258 · 2002-05-10

Decision Date2002-05-10
Product CodeMCF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Germ Terminator Corporation. It received FDA 510(k) clearance on 2002-05-10 under 510(k) number K021258. 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 GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER?

GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER is a medical device that received FDA 510(k) clearance on 2002-05-10. The listed applicant is Germ Terminator Corporation. The 510(k) number is K021258.

When did GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER receive FDA 510(k) clearance?

GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER received FDA 510(k) clearance on 2002-05-10, under 510(k) number K021258.

Who is the listed applicant for GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER?

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

What is the FDA product code for GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER?

The FDA product code for GERM TERMINATOR GT 100 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.

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.

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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