AMG PMP Pediatric
K-Number: K202206 · 2021-04-01
Device Summary
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. The listed applicant is Eurosets S.R.L. The 510(k) number is K202206.
When did AMG PMP Pediatric receive FDA 510(k) clearance?
AMG PMP Pediatric received FDA 510(k) clearance on 2021-04-01, under 510(k) number K202206.
Who is the listed applicant for AMG PMP Pediatric?
The FDA 510(k) record lists Eurosets S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMG PMP Pediatric?
The FDA product code for AMG PMP Pediatric is DTZ.
Other records listing Eurosets S.R.L 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: DTZ)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.