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FDA 510(k)

PLAQUE DETECTION SYSTEM

K-Number: K781919 · 1978-12-04

ApplicantClairol, Inc.
Decision Date1978-12-04
Product CodeNYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAQUE DETECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Clairol, Inc.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781919. The device is classified under product code NYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAQUE DETECTION SYSTEM?

PLAQUE DETECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Clairol, Inc.. The 510(k) number is K781919.

When did PLAQUE DETECTION SYSTEM receive FDA 510(k) clearance?

PLAQUE DETECTION SYSTEM received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781919.

Who is the listed applicant for PLAQUE DETECTION SYSTEM?

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

What is the FDA product code for PLAQUE DETECTION SYSTEM?

The FDA product code for PLAQUE DETECTION SYSTEM is NYH.

Related Clinical Trials

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Other records listing Clairol, 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.

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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.

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