Belmont Equipment Corp. is one of 10021 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Belmont Equipment Corp. - FDA 510(k) Cleared Devices
Recent clearances: BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIES, BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY
12
Total
12
Cleared
0
Denied
Belmont Equipment Corp. has 12 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1981 to 2000.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Belmont Equipment Corp.
12 devices
Cleared
May 17, 2000
BELMONT UNIT, MODEL 2000 SERIES
Dental
65d
Cleared
Jan 12, 1999
BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIES
Dental
85d
Cleared
Dec 23, 1996
BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY
Radiology
98d
Cleared
May 23, 1990
PANORAMIC MODEL X-CALIBER X-RAY
Radiology
100d
Cleared
Dec 07, 1987
MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY
Radiology
53d
Cleared
Mar 25, 1987
BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75
Radiology
56d
Cleared
Apr 24, 1986
NEW BELMONT MODEL, MC-5 DENTAL, INTRAORAL X-RAY
Radiology
15d
Cleared
Jun 05, 1985
BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD
Radiology
28d
Cleared
Feb 21, 1985
BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG
Radiology
92d
Cleared
Dec 29, 1983
ACURAY 071A DENTAL INTRAORAL X-RAY
Radiology
37d
Cleared
Sep 12, 1983
ACURACY 071, DENTAL, INTRAORAL-X-RAY
Radiology
77d
Cleared
Jun 09, 1981
BELMONT PODIATRY MODEL 065 X-RAY
Radiology
43d