Pie Data, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pie Data, Inc. makes
Pie Data, Inc. manufactures the SCANNER 560, an ultrasound scanner designed for medical imaging, and the VIDEO IMAGE PROCESSOR, a device for enhancing and analyzing ultrasound video signals.
The company’s products are regulated under the FDA’s 510(k) pathway in the United States. The SCANNER 560 and VIDEO IMAGE PROCESSOR are listed in the FDA’s 510(k) database, reflecting their classification as Class II medical devices.
Catalogue
Scanner 560 Ultrasound Scanner Ref K827713
Regimes: 510(k) Registry: 510(k)Video Image Processor Ref K828621
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pie Data, Inc. have in the registry?
The registry currently lists 2 devices for Pie Data, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pie Data, Inc.'s devices?
Among its 2 most recently registered devices, Pie Data, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Pie Data, Inc. in the registry?
The most recently registered devices listed for Pie Data, Inc. include SCANNER 560 ULTRASOUND SCANNER and VIDEO IMAGE PROCESSOR.