510(k) K852019

BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD by Belmont Equipment Corp. — Product Code EAP

K852019 is an FDA 510(k) premarket notification submitted by Belmont Equipment Corp. for the device "BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD". The FDA issued a decision of Substantially Equivalent on June 5, 1985. 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
June 5, 1985
Date Received
May 8, 1985
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