ACURACY 071, DENTAL, INTRAORAL-X-RAY
K-Number: K832065 · 1983-09-12
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Device Summary
Frequently Asked Questions
What is the ACURACY 071, DENTAL, INTRAORAL-X-RAY?
ACURACY 071, DENTAL, INTRAORAL-X-RAY is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K832065.
When did ACURACY 071, DENTAL, INTRAORAL-X-RAY receive FDA 510(k) clearance?
ACURACY 071, DENTAL, INTRAORAL-X-RAY received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832065.
Who is the listed applicant for ACURACY 071, DENTAL, INTRAORAL-X-RAY?
The FDA 510(k) record lists Belmont Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACURACY 071, DENTAL, INTRAORAL-X-RAY?
The FDA product code for ACURACY 071, DENTAL, INTRAORAL-X-RAY 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 Belmont Equipment 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: 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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