FDA 510(k)

AURO-BRUSH

K-Number: K781351 · 1978-12-04

Decision Date1978-12-04

Product Code

DecisionSubstantially Equivalent

Device Summary

AURO-BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781351. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AURO-BRUSH?

AURO-BRUSH is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K781351.

When did AURO-BRUSH receive FDA 510(k) clearance?

AURO-BRUSH received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781351.

Who is the listed applicant for AURO-BRUSH?

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

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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.