Kli is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kli - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Kli has 18 FDA 510(k) cleared obstetrics & gynecology devices. Based in Walker, US.
Historical record: 18 cleared submissions from 1977 to 1980.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kli
18 devices
Cleared
Jun 17, 1980
CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE
Gastroenterology & Urology
64d
Cleared
May 14, 1980
GYNECOLOGICAL CYSTO/URETHROSCOPE
Gastroenterology & Urology
23d
Cleared
Dec 04, 1978
INSUFFALATOR LAPARAOSCOPIC
Obstetrics & Gynecology
20d
Cleared
Sep 14, 1978
FORCEPS, ELECTROSURGICAL
Obstetrics & Gynecology
76d
Cleared
Jul 17, 1978
ONE INCISION BI-POLAR ELECTRO. FORCEPS
Obstetrics & Gynecology
18d
Cleared
Jun 22, 1978
SCISSORS, HOOK, ELECTROSURGICAL
Obstetrics & Gynecology
13d
Cleared
Jun 22, 1978
SCISSORS, HOOK, ELECTROSURGICAL
Obstetrics & Gynecology
13d
Cleared
Jan 05, 1978
INSUFFLATOR, MODEL G100 & 200
Obstetrics & Gynecology
23d
Cleared
Dec 20, 1977
LAPAROSCOPY CONSOLE MODEL VIII
Obstetrics & Gynecology
12d
Cleared
Dec 13, 1977
PROBE, COAGULATION ACCESSORY
Obstetrics & Gynecology
8d
Cleared
Nov 30, 1977
LAPAROSCOPE W/REMOVABLE OPTICS
Obstetrics & Gynecology
5d
Cleared
Nov 21, 1977
CAMERA ADAPTER FOR ENDOSCOPES
Obstetrics & Gynecology
35d