Capintec Instruments, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Capintec Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 7 cleared submissions from 1991 to 1994. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Capintec Instruments, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Sep 29, 1994
BETA C COUNTER
Radiology
93d
Cleared
Feb 18, 1994
CAPINTEC CRC 35R
Radiology
94d
Cleared
May 18, 1993
CAPTUS 2000 WEL COUNTER
Radiology
83d
Cleared
Dec 03, 1992
CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWARE
Radiology
84d
Cleared
May 28, 1992
CAPTUS 500
Radiology
65d
Cleared
Apr 08, 1991
CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS
Radiology
95d
Cleared
Mar 18, 1991
DOSE CALIBRATOR
Radiology
81d