Varian, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Ontrak Testcup Ii And Onsite Cupkit Ref K033902
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Ontrak Testcard 9 Ref K050321
Regimes: 510(k) Registry: 510(k)Varian, Inc. Ontrak Testcup And Ontrak Teststik Ref K033659
Regimes: 510(k) Registry: 510(k)On Trak Testcard Ref K051235
Regimes: 510(k) Registry: 510(k)
FDA recalls
2003
- 18 Jul 2003 Z-1202-03 Unclassified (pre-2012) Terminated Stability in question.
Frequently asked questions
How many devices does Varian, Inc. have in the registry?
The registry currently lists 5 devices for Varian, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Varian, Inc.'s devices?
Among its 5 most recently registered devices, Varian, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Varian, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Varian, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Varian, Inc.?
FDA recall records list 1 recall initiated by Varian, Inc., the most recent initiated on 18 Jul 2003. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Varian, Inc. in the registry?
The most recently registered devices listed for Varian, Inc. include ONTRAK TESTCUP II AND ONSITE CUPKIT, MODIFICATION TO ONTRAK TESTCUP II AND ONSITE CUPKIT, ONTRAK TESTCARD 9 and VARIAN, INC. ONTRAK TESTCUP AND ONTRAK TESTSTIK.