Conceptus, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cervical Catheter Ref K933981
Regimes: 510(k) Registry: 510(k)Intrauterine Catheter And Introducer Ref K932993
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Conceptus Vari-Soft Cath/Pirouette Posit Mandrel Ref K932387
Regimes: 510(k) Registry: 510(k)Hysteroscope Ref K954164
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Conceptus Fallopian Tube Catheterization System Ref K953314
Regimes: 510(k) Registry: 510(k)Resectoscope Safety Sheath Ref K972210
Regimes: 510(k) Registry: 510(k)Conceptus Uterine Catheter Ref K933723
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Conceptus, Inc. have in the registry?
The registry currently lists 9 devices for Conceptus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Conceptus, Inc.'s devices?
Among its 9 most recently registered devices, Conceptus, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Conceptus, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Conceptus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Conceptus, Inc. in the registry?
The most recently registered devices listed for Conceptus, Inc. include CERVICAL CATHETER, INTRAUTERINE CATHETER AND INTRODUCER, STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBING and CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL.