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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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