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FDA 510(k)

AMG PMP Pediatric

K-Number: K202206 · 2021-04-01

Decision Date2021-04-01
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMG PMP Pediatric is a medical device manufactured by Eurosets S.R.L. It received FDA 510(k) clearance on 2021-04-01 under approval number K202206. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMG PMP Pediatric?

AMG PMP Pediatric is a medical device that received FDA 510(k) clearance on 2021-04-01. It is manufactured by Eurosets S.R.L. The 510(k) number is K202206.

When was AMG PMP Pediatric approved by the FDA?

AMG PMP Pediatric received FDA 510(k) clearance on 2021-04-01, under approval number K202206.

What company makes AMG PMP Pediatric?

AMG PMP Pediatric is manufactured by Eurosets S.R.L.

What is the FDA product code for AMG PMP Pediatric?

The FDA product code for AMG PMP Pediatric is DTZ.

Other Devices by Eurosets S.R.L

Related Devices (Code: DTZ)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.