Wyeth-Ayerst Laboratories, Inc.
Country not established
- Devices
- 1
What Wyeth-Ayerst Laboratories, Inc. makes
Wyeth-Ayerst Laboratories, Inc. manufactures the NORPLANT® trocar, a device used for subcutaneous insertion of contraceptive implants.
The NORPLANT® trocar is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Norplant(R) Trocar Ref K903490
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wyeth-Ayerst Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Wyeth-Ayerst Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wyeth-Ayerst Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Wyeth-Ayerst Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wyeth-Ayerst Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wyeth-Ayerst Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wyeth-Ayerst Laboratories, Inc. in the registry?
The most recently registered devices listed for Wyeth-Ayerst Laboratories, Inc. include NORPLANT(R) TROCAR.