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FDA 510(k)

KERR COMMAND ULTRAFINE POLISHING PASTE

K-Number: K843022 · 1984-08-24

Decision Date1984-08-24
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR COMMAND ULTRAFINE POLISHING PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation (Danbury). It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K843022. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERR COMMAND ULTRAFINE POLISHING PASTE?

KERR COMMAND ULTRAFINE POLISHING PASTE is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K843022.

When did KERR COMMAND ULTRAFINE POLISHING PASTE receive FDA 510(k) clearance?

KERR COMMAND ULTRAFINE POLISHING PASTE received FDA 510(k) clearance on 1984-08-24, under 510(k) number K843022.

Who is the listed applicant for KERR COMMAND ULTRAFINE POLISHING PASTE?

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

What is the FDA product code for KERR COMMAND ULTRAFINE POLISHING PASTE?

The FDA product code for KERR COMMAND ULTRAFINE POLISHING PASTE is EJR.

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 Kerr Corporation (Danbury) 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 32 devices →

Related Devices (Code: EJR)

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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