FDA 510(k) Applications Submitted by BELMONT EQUIPMENT CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K000799 03/13/2000 BELMONT UNIT, MODEL 2000 SERIES BELMONT EQUIPMENT CORP.
K963699 09/16/1996 BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY BELMONT EQUIPMENT CORP.
K983661 10/19/1998 BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIES BELMONT EQUIPMENT CORP.


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