NovaPACS
K-Number: K171754 · 2017-07-28
ApplicantNovarad Corporation
Decision Date2017-07-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
NovaPACS is a medical device manufactured by Novarad Corporation. It received FDA 510(k) clearance on 2017-07-28 under approval number K171754. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NovaPACS?
NovaPACS is a medical device that received FDA 510(k) clearance on 2017-07-28. It is manufactured by Novarad Corporation. The 510(k) number is K171754.
When was NovaPACS approved by the FDA?
NovaPACS received FDA 510(k) clearance on 2017-07-28, under approval number K171754.
What company makes NovaPACS?
NovaPACS is manufactured by Novarad Corporation.
What is the FDA product code for NovaPACS?
The FDA product code for NovaPACS is LLZ.
Other Devices by Novarad Corporation
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.