Conceptus, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conceptus, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Conceptus, Inc. has 9 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 9 cleared submissions from 1994 to 1998. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Conceptus, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conceptus, Inc.
9 devices
Cleared
Jan 21, 1998
STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBING
Obstetrics & Gynecology
90d
Cleared
Sep 05, 1997
RESECTOSCOPE SAFETY SHEATH
Obstetrics & Gynecology
86d
Cleared
Jan 31, 1997
CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
Obstetrics & Gynecology
214d
Cleared
Mar 12, 1996
HYSTEROSCOPE
Obstetrics & Gynecology
189d
Cleared
Jul 28, 1995
CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM
Obstetrics & Gynecology
16d
Cleared
Mar 06, 1995
CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL
Obstetrics & Gynecology
658d
Cleared
Jan 06, 1995
INTRAUTERINE CATHETER AND INTRODUCER
Obstetrics & Gynecology
567d
Cleared
Dec 27, 1994
CONCEPTUS UTERINE CATHETER
Obstetrics & Gynecology
512d
Cleared
Dec 27, 1994
CERVICAL CATHETER
Obstetrics & Gynecology
498d