Farrall Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Farrall Instruments, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Farrall Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1976 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Farrall Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Farrall Instruments, Inc.
7 devices
Cleared
Jan 10, 1995
CAT-600 PENILE PLETHYSMOGRAPH
Gastroenterology & Urology
690d
Cleared
Jan 10, 1995
CAT-400UL PENILE PLETHYSMOGRAPH
Gastroenterology & Urology
365d
Cleared
Sep 15, 1982
BI-4520 DUAL IMPEDOMETER
General & Plastic Surgery
98d
Cleared
Jul 13, 1982
PP-100, PERSONAL PERINEOMETER
Gastroenterology & Urology
46d
Cleared
Dec 20, 1979
A SLEEP ASSESSMENT DEVICE
Neurology
34d
Cleared
Oct 03, 1978
VISUALAX
Neurology
11d
Cleared
Jul 20, 1976
STIMULATOR, SONIC CONTROL (AS-1)
Neurology
14d