Kinetic Medical Products - FDA 510(k) Cleared Devices
63
Total
63
Cleared
0
Denied
Kinetic Medical Products has 63 FDA 510(k) cleared medical devices. Based in Erie, US.
Historical record: 63 cleared submissions from 1989 to 1989. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kinetic Medical Products Filter by specialty or product code using the sidebar.
63 devices
Cleared
Mar 01, 1989
MIDWIFERY/OBSTETRICAL FORCEPS
Obstetrics & Gynecology
37d
Cleared
Feb 27, 1989
VAGINAL SPECULUM
Obstetrics & Gynecology
35d
Cleared
Feb 27, 1989
CERVICAL BIOPSY FORCEPS
Obstetrics & Gynecology
35d
Cleared
Feb 27, 1989
COMPRESSION FORCEPS
Obstetrics & Gynecology
35d
Cleared
Feb 27, 1989
MALLEABLE PLACENTA CURETTE
Obstetrics & Gynecology
35d
Cleared
Feb 16, 1989
MICROSURGICAL KERATOME
Neurology
29d
Cleared
Feb 16, 1989
HYSTERECTOMY FORCEPS
Obstetrics & Gynecology
24d
Cleared
Feb 13, 1989
VAGINAL SPECULUM
Obstetrics & Gynecology
21d
Cleared
Feb 13, 1989
FIXED-SIZE UTERINE DILATOR
Obstetrics & Gynecology
21d
Cleared
Feb 13, 1989
UTERINE DRESSING FORCEPS
Obstetrics & Gynecology
21d
Cleared
Feb 13, 1989
UTERINE TENTACULUM
Obstetrics & Gynecology
21d
Cleared
Feb 13, 1989
UTERINE CURETTE
Obstetrics & Gynecology
21d
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