TPE DIAMOND POINTS
K-Number: K832855 · 1983-09-29
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Device Summary
Frequently Asked Questions
What is the TPE DIAMOND POINTS?
TPE DIAMOND POINTS is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Shofu Dental Corp.. The 510(k) number is K832855.
When did TPE DIAMOND POINTS receive FDA 510(k) clearance?
TPE DIAMOND POINTS received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832855.
Who is the listed applicant for TPE 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 TPE DIAMOND POINTS?
The FDA product code for TPE 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.
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
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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