Victus, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Extension Set (Standardbore Tubing), Extension Set (Minibore Tubing), Iv Administration Set ( Standard Ref K093271
Regimes: 510(k) Registry: 510(k)
FDA recalls
2011
- 20 Sep 2011 Z-0080-2012 Unclassified (pre-2012) Terminated Victus, Inc. Miami, FL is recalling Vipat Brand Elastomeric Infusion Pump, Model H0020-100, Lot 100533. The product may have a higher flow rate than specified. The use of this product may lead to over-administration of drug solutions to patients.
Frequently asked questions
How many devices does Victus, Inc. have in the registry?
The registry currently lists 3 devices for Victus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Victus, Inc.'s devices?
Among its 3 most recently registered devices, Victus, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Victus, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Victus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Victus, Inc.?
FDA recall records list 1 recall initiated by Victus, Inc., the most recent initiated on 20 Sep 2011. 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 Victus, Inc. in the registry?
The most recently registered devices listed for Victus, Inc. include VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059, 27062, VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072 and EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE TUBING), IV ADMINISTRATION SET ( STANDARD.