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FDA 510(k)

DS60 TOOTHBRUSH SANITIZER

K-Number: K901459 · 1990-09-17

Decision Date1990-09-17
Product CodeMCF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DS60 TOOTHBRUSH SANITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Associated Mills, Inc.. It received FDA 510(k) clearance on 1990-09-17 under 510(k) number K901459. 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 DS60 TOOTHBRUSH SANITIZER?

DS60 TOOTHBRUSH SANITIZER is a medical device that received FDA 510(k) clearance on 1990-09-17. The listed applicant is Associated Mills, Inc.. The 510(k) number is K901459.

When did DS60 TOOTHBRUSH SANITIZER receive FDA 510(k) clearance?

DS60 TOOTHBRUSH SANITIZER received FDA 510(k) clearance on 1990-09-17, under 510(k) number K901459.

Who is the listed applicant for DS60 TOOTHBRUSH SANITIZER?

The FDA 510(k) record lists Associated Mills, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DS60 TOOTHBRUSH SANITIZER?

The FDA product code for DS60 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.

Other records listing Associated Mills, Inc. 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.

View all 14 devices →

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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