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FDA 510(k)

EAR CURETTE, VARIOUS

K-Number: K841001 · 1984-05-29

Decision Date1984-05-29
Product CodeJYG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EAR CURETTE, VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1984-05-29 under 510(k) number K841001. The device is classified under product code JYG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAR CURETTE, VARIOUS?

EAR CURETTE, VARIOUS is a medical device that received FDA 510(k) clearance on 1984-05-29. The listed applicant is Premier Dental Products Co.. The 510(k) number is K841001.

When did EAR CURETTE, VARIOUS receive FDA 510(k) clearance?

EAR CURETTE, VARIOUS received FDA 510(k) clearance on 1984-05-29, under 510(k) number K841001.

Who is the listed applicant for EAR CURETTE, VARIOUS?

The FDA 510(k) record lists Premier Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EAR CURETTE, VARIOUS?

The FDA product code for EAR CURETTE, VARIOUS is JYG.

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 Premier Dental Products Co. 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 40 devices →

Related Devices (Code: JYG)

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

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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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