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FDA 510(k)

BRUSHRITE

K-Number: K880442 · 1988-05-16

ApplicantPro Care Laboratories, Inc.
Decision Date1988-05-16
Product CodeJEG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BRUSHRITE is the device name listed in this FDA 510(k) record. The listed applicant is Pro Care Laboratories, Inc.. It received FDA 510(k) clearance on 1988-05-16 under 510(k) number K880442. The device is classified under product code JEG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUSHRITE?

BRUSHRITE is a medical device that received FDA 510(k) clearance on 1988-05-16. The listed applicant is Pro Care Laboratories, Inc.. The 510(k) number is K880442.

When did BRUSHRITE receive FDA 510(k) clearance?

BRUSHRITE received FDA 510(k) clearance on 1988-05-16, under 510(k) number K880442.

Who is the listed applicant for BRUSHRITE?

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

What is the FDA product code for BRUSHRITE?

The FDA product code for BRUSHRITE is JEG.

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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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