Accutome, Inc. is one of 14224 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accutome, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 4Sight, ACCUTIP COVER, A-SCAN PLUS CONNECT
8
Total
8
Cleared
0
Denied
Accutome, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1981 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Accutome, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Accutome, Inc.
8 devices
Cleared
Nov 25, 2015
4Sight
Radiology
77d
Cleared
Apr 23, 2014
ACCUTIP COVER
Ophthalmic
252d
Cleared
Jan 29, 2013
A-SCAN PLUS CONNECT
Radiology
90d
Cleared
Mar 14, 2011
UBM PLUS
Radiology
110d
Cleared
Mar 28, 2005
PACHPEN PACHYMETER, MODEL 24-5100
Radiology
25d
Cleared
Oct 10, 2003
ACCUSONIC A-SCAN MODEL, 24-4000
Radiology
18d
Cleared
Feb 24, 1982
KREMER BLADE GAUGE
Ophthalmic
47d
Cleared
Aug 21, 1981
KREMER CORNEOMETER ULTRASONIC PACHOMETER
Radiology
163d