X-RAY UNIT, DENTAL DIAGNOSTIC
K-Number: K760323 · 1976-08-03
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Device Summary
Frequently Asked Questions
What is the X-RAY UNIT, DENTAL DIAGNOSTIC?
X-RAY UNIT, DENTAL DIAGNOSTIC is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is The S. S. White Co.. The 510(k) number is K760323.
When did X-RAY UNIT, DENTAL DIAGNOSTIC receive FDA 510(k) clearance?
X-RAY UNIT, DENTAL DIAGNOSTIC received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760323.
Who is the listed applicant for X-RAY UNIT, DENTAL DIAGNOSTIC?
The FDA 510(k) record lists The S. S. White Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-RAY UNIT, DENTAL DIAGNOSTIC?
The FDA product code for X-RAY UNIT, DENTAL DIAGNOSTIC is EAP.
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 The S. S. White 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.
Related Devices (Code: EAP)
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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