Transamerica Delaval, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Transamerica Delaval, Inc. makes
Transamerica Delaval, Inc. manufactures medical devices including flush devices, automatic flush devices, and disposable pressure transducer systems. Their product line also consists of administration sets, stopcocks, monitoring kits, and sterile disposable domes.
These devices are classified as Class II medical products and are listed within the FDA 510(k) regulatory registry. The company is based in the United States.
Catalogue
Flush Device Ref K833170
Regimes: 510(k) Registry: 510(k)Disposable Pressure Transducer System Sterile Ref K853996
Regimes: 510(k) Registry: 510(k)Administration Set Ref K851988
Regimes: 510(k) Registry: 510(k)Flush Device, Automatic Ref K851987
Regimes: 510(k) Registry: 510(k)Stopcocks Ref K851986
Regimes: 510(k) Registry: 510(k)Monitoring Kit Ref K833171
Regimes: 510(k) Registry: 510(k)Dome, Disposable, Sterile Ref K851989
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transamerica Delaval, Inc. have in the registry?
The registry currently lists 7 devices for Transamerica Delaval, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transamerica Delaval, Inc.'s devices?
Among its 7 most recently registered devices, Transamerica Delaval, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Transamerica Delaval, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Transamerica Delaval, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transamerica Delaval, Inc. in the registry?
The most recently registered devices listed for Transamerica Delaval, Inc. include FLUSH DEVICE, DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE, ADMINISTRATION SET and FLUSH DEVICE, AUTOMATIC.