Aveta System
K-Number: K191958 · 2019-10-01
ApplicantMeditrina, Inc.
Decision Date2019-10-01
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Aveta System is a medical device manufactured by Meditrina, Inc.. It received FDA 510(k) clearance on 2019-10-01 under approval number K191958. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aveta System?
Aveta System is a medical device that received FDA 510(k) clearance on 2019-10-01. It is manufactured by Meditrina, Inc.. The 510(k) number is K191958.
When was Aveta System approved by the FDA?
Aveta System received FDA 510(k) clearance on 2019-10-01, under approval number K191958.
What company makes Aveta System?
Aveta System is manufactured by Meditrina, Inc..
What is the FDA product code for Aveta System?
The FDA product code for Aveta System is HIH.
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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.