Advanced Technology Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Technology Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Q LAB SOFTWARE, HDI 5000 ULTRASOUND SYSTEM WITH ASSISTED BORDER DETECTION (ABD), XRES IMAGING, AND PANORAMIC MEASUREMENT CAPABILITY, MEDLINK DIAGNOSTIC OFFLINE WORKSTATION
61
Total
59
Cleared
0
Denied
Advanced Technology Laboratories, Inc. has 59 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 59 cleared submissions from 1980 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Advanced Technology Laboratories, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Product Service, Inc. and Tuv America, Inc..
FDA 510(k) Regulatory Record - Advanced Technology Laboratories, Inc.
61 devices
Cleared
Jul 02, 2002
Q LAB SOFTWARE
Radiology
15d
Cleared
May 04, 2001
HDI 5000 ULTRASOUND SYSTEM WITH ASSISTED BORDER DETECTION (ABD), XRES...
Radiology
14d
Cleared
Sep 28, 2000
MEDLINK DIAGNOSTIC OFFLINE WORKSTATION
Radiology
73d
Cleared
Aug 23, 1999
ULTRAMARK 400C/SONOACE 6000 ULTRASOUND SYSTEM
Radiology
28d
Cleared
Jun 18, 1999
HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
32d
Cleared
Mar 26, 1997
LEVEL 10 HDI
Radiology
344d
Cleared
Oct 11, 1994
PEGASUS
Radiology
356d
Cleared
Jul 29, 1994
NOVA MICROSONICS ACCESS IMAGE MANAGEMENT NETWORK/ACCESS ACQUISITION MODULE
Radiology
179d
Cleared
Feb 28, 1991
NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS
Cardiovascular
99d
Cleared
Feb 26, 1991
ULTRAMARK 9 ULTRASOUND SYSTEM (UM 9)
Radiology
202d
Cleared
Nov 23, 1990
CEPHALIC DOPPLER W/ULTRAMARK 9 ULTRASOUND SYSTEM
Radiology
247d
Cleared
Nov 08, 1990
BIOPSY NEEDLE TRANSPONDER SYSTEM
Radiology
176d
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