Prudent 1717, Prudent 1417, Prudent 1212
K-Number: K211108 · 2021-06-04
ApplicantPixxgen Corporation
Decision Date2021-06-04
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Prudent 1717, Prudent 1417, Prudent 1212 is a medical device manufactured by Pixxgen Corporation. It received FDA 510(k) clearance on 2021-06-04 under approval number K211108. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Prudent 1717, Prudent 1417, Prudent 1212?
Prudent 1717, Prudent 1417, Prudent 1212 is a medical device that received FDA 510(k) clearance on 2021-06-04. It is manufactured by Pixxgen Corporation. The 510(k) number is K211108.
When was Prudent 1717, Prudent 1417, Prudent 1212 approved by the FDA?
Prudent 1717, Prudent 1417, Prudent 1212 received FDA 510(k) clearance on 2021-06-04, under approval number K211108.
What company makes Prudent 1717, Prudent 1417, Prudent 1212?
Prudent 1717, Prudent 1417, Prudent 1212 is manufactured by Pixxgen Corporation.
What is the FDA product code for Prudent 1717, Prudent 1417, Prudent 1212?
The FDA product code for Prudent 1717, Prudent 1417, Prudent 1212 is MQB.
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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.