Telos Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Telos Medical Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Telos Medical Corp. has 7 FDA 510(k) cleared medical devices. Based in Keene, US.
Historical record: 7 cleared submissions from 1988 to 1992. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Telos Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Telos Medical Corp.
7 devices
Cleared
Oct 27, 1992
DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER
Obstetrics & Gynecology
272d
Cleared
Apr 03, 1992
DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT
Obstetrics & Gynecology
88d
Cleared
Dec 30, 1991
TRANSCERVICAL INTRAUTERINE KIT
Obstetrics & Gynecology
90d
Cleared
Jan 16, 1991
LAB-SITE SAFETY NEEDLE
Cardiovascular
70d
Cleared
Jan 15, 1991
LAB-SITE
Cardiovascular
69d
Cleared
Oct 12, 1989
ULTRANS DISPOSABLE INTRAUTERINE
Obstetrics & Gynecology
504d
Cleared
Dec 13, 1988
CATHETER, INTRAUTERINE AND INTRODUCER
Obstetrics & Gynecology
95d