Medical Device Manufacturer · US , Sound Beach , NY

Schick Technologies, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1994
13
Total
13
Cleared
0
Denied

Schick Technologies, Inc. has 13 FDA 510(k) cleared radiology devices. Based in Sound Beach, US.

Historical record: 13 cleared submissions from 1994 to 2011.

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 - Schick Technologies, Inc.
13 devices
1-13 of 13
Cleared Apr 20, 2011
COMPUTED DENTAL RADIOGRAPHY
K110768 · MUH
Radiology · 33d
Cleared Nov 30, 2009
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
K093453 · EAP
Radiology · 25d
Cleared Nov 02, 2007
SCHICK COMPUTED ORAL RADIOLOGY SYSTEM
K072134 · MUH
Radiology · 92d
Cleared Feb 17, 2006
CEPH, MODEL 4900
K053558 · MUH
Radiology · 58d
Cleared Jun 07, 2004
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
K041385 · EAP
Radiology · 13d
Cleared May 05, 2003
CDR PANX, MODEL 4792
K031291 · MUH
Radiology · 12d
Cleared Oct 02, 2002
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
K022953 · MUH
Radiology · 27d
Cleared May 26, 2000
MODIFICATION TO ACCUDEXA BONE DENSITOMETER
K001429 · KGI
Radiology · 21d
Cleared Dec 11, 1998
CDR - PAN MODEL 4700
K982661 · MQB
Radiology · 134d
Cleared Jun 04, 1998
ACCUDEXA BONE DENSITOMETER
K981124 · KGI
Radiology · 69d
Cleared Dec 02, 1997
ACCUDEXA BONE DENSITOMETER
K971735 · KGI
Radiology · 204d
Cleared Nov 22, 1996
CDR-CAM
K963778 · EIA
Dental · 63d
Cleared Jan 31, 1994
COMPUTED ORAL RADIOLOGY SYSTEM
K933455 · EAP
Radiology · 201d
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