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FDA 510(k)

GINGI CURETTAGE DIAMOND POINTS

K-Number: K832856 · 1983-10-04

Decision Date1983-10-04
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GINGI CURETTAGE DIAMOND POINTS is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832856. The device is classified under product code DZP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GINGI CURETTAGE DIAMOND POINTS?

GINGI CURETTAGE DIAMOND POINTS is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Shofu Dental Corp.. The 510(k) number is K832856.

When did GINGI CURETTAGE DIAMOND POINTS receive FDA 510(k) clearance?

GINGI CURETTAGE DIAMOND POINTS received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832856.

Who is the listed applicant for GINGI CURETTAGE DIAMOND POINTS?

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

What is the FDA product code for GINGI CURETTAGE DIAMOND POINTS?

The FDA product code for GINGI CURETTAGE DIAMOND POINTS is DZP.

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 Shofu Dental Corp. 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 59 devices →

Related Devices (Code: DZP)

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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