BEACH CURETTE NO. 2 AND NO. 3 T.G.
K-Number: K821789 · 1982-07-06
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Device Summary
Frequently Asked Questions
What is the BEACH CURETTE NO. 2 AND NO. 3 T.G.?
BEACH CURETTE NO. 2 AND NO. 3 T.G. is a medical device that received FDA 510(k) clearance on 1982-07-06. The listed applicant is Pacific Dental Corp.. The 510(k) number is K821789.
When did BEACH CURETTE NO. 2 AND NO. 3 T.G. receive FDA 510(k) clearance?
BEACH CURETTE NO. 2 AND NO. 3 T.G. received FDA 510(k) clearance on 1982-07-06, under 510(k) number K821789.
Who is the listed applicant for BEACH CURETTE NO. 2 AND NO. 3 T.G.?
The FDA 510(k) record lists Pacific Dental Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEACH CURETTE NO. 2 AND NO. 3 T.G.?
The FDA product code for BEACH CURETTE NO. 2 AND NO. 3 T.G. is EMS.
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 Pacific 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: EMS)
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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