Simpson/Basye, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Simpson/Basye, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Simpson/Basye, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1978 to 1994. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Simpson/Basye, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Simpson/Basye, Inc.
12 devices
Cleared
Mar 25, 1994
SEDLACEK HANDLE
Obstetrics & Gynecology
472d
Cleared
Jun 23, 1989
MARLOW ANAL SPECULUM
Gastroenterology & Urology
105d
Cleared
May 11, 1989
NEWPORT LATERAL VAGINAL RETRACTOR
Obstetrics & Gynecology
62d
Cleared
Mar 29, 1989
REID ENDOCERVICAL SPREADER
Obstetrics & Gynecology
19d
Cleared
Mar 29, 1989
CAMPION CERVICAL HOOK
Obstetrics & Gynecology
19d
Cleared
Mar 29, 1989
NEWPORT CERVICAL MANIPULATOR
Obstetrics & Gynecology
19d
Cleared
Mar 22, 1989
CAMPION LASER FORCEPS
General & Plastic Surgery
12d
Cleared
May 07, 1987
HEATED INSTRUMENT BATH
General Hospital
100d
Cleared
Jul 30, 1986
HAND MIRROR (ENDOSCOPE)
Gastroenterology & Urology
13d
Cleared
Jul 17, 1986
SURGICAL LASER ACCESSORIES (SLA) CASE
General & Plastic Surgery
7d
Cleared
Jun 22, 1979
MI-MARK ENDOCERVICAL SAMPLING SET
Obstetrics & Gynecology
38d
Cleared
Mar 02, 1978
SEXUAL ASSAULT FORENCIC EVIDENCE KIT
General Hospital
79d