VERIQA
K-Number: K213370 · 2022-03-30
Decision Date2022-03-30
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VERIQA is a medical device manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten. It received FDA 510(k) clearance on 2022-03-30 under approval number K213370. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VERIQA?
VERIQA is a medical device that received FDA 510(k) clearance on 2022-03-30. It is manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten. The 510(k) number is K213370.
When was VERIQA approved by the FDA?
VERIQA received FDA 510(k) clearance on 2022-03-30, under approval number K213370.
What company makes VERIQA?
VERIQA is manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten.
What is the FDA product code for VERIQA?
The FDA product code for VERIQA is IYE.
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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.