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FDA 510(k)

Aveta System

K-Number: K191958 · 2019-10-01

Decision Date2019-10-01
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Aveta System is the device name listed in this FDA 510(k) record. The listed applicant is Meditrina, Inc.. It received FDA 510(k) clearance on 2019-10-01 under 510(k) 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. The listed applicant is Meditrina, Inc.. The 510(k) number is K191958.

When did Aveta System receive FDA 510(k) clearance?

Aveta System received FDA 510(k) clearance on 2019-10-01, under 510(k) number K191958.

Who is the listed applicant for Aveta System?

The FDA 510(k) record lists Meditrina, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aveta System?

The FDA product code for Aveta System is HIH.

Other records listing Meditrina, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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