510(k) K832065

ACURACY 071, DENTAL, INTRAORAL-X-RAY by Belmont Equipment Corp. — Product Code EAP

K832065 is an FDA 510(k) premarket notification submitted by Belmont Equipment Corp. for the device "ACURACY 071, DENTAL, INTRAORAL-X-RAY". The FDA issued a decision of Substantially Equivalent on September 12, 1983. The device falls under product code EAP (Unit, X-Ray, Intraoral), a Class II device regulated under 21 CFR 872.1810. Belmont Equipment Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 12, 1983
Date Received
June 27, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, X-Ray, Intraoral
Device Class
Class II
Regulation Number
872.1810
Review Panel
RA
Submission Type