DLP Medical Products, Corp.
Country not established FDA establishment FEI 3027534634
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Insulin syringe with integrated needle DL Ref K203211
510(k) 510(k)
Company details
- FDA FEI number
- 3027534634
- Address
- 203 S St Mary's St, Suite 160, San Antonio, TX, 78205
Frequently asked questions
How many devices does DLP Medical Products, Corp. have in the registry?
The registry currently lists 1 device for DLP Medical Products, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list DLP Medical Products, Corp.'s devices?
Among its 1 most recently registered device, DLP Medical Products, Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do DLP Medical Products, Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for DLP Medical Products, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DLP Medical Products, Corp. in the registry?
The most recently registered devices listed for DLP Medical Products, Corp. include Insulin syringe with integrated needle DL.