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FDA PMA

OCCLUDER, PATENT DUCTUS, ARTERIOSUS

PMA Number: P120009 · 2024-10-17

ApplicantPfm Medical, Inc.
Decision Date2024-10-17
PMA NumberP120009
Product CodeMAE
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

OCCLUDER, PATENT DUCTUS, ARTERIOSUS is the device name listed in this FDA 510(k) record. The listed applicant is Pfm Medical, Inc.. It received FDA 510(k) clearance on 2024-10-17. The device is classified under product code MAE. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the OCCLUDER, PATENT DUCTUS, ARTERIOSUS?

OCCLUDER, PATENT DUCTUS, ARTERIOSUS is a medical device that received FDA 510(k) clearance on 2024-10-17. The listed applicant is Pfm Medical, Inc..

When did OCCLUDER, PATENT DUCTUS, ARTERIOSUS receive FDA 510(k) clearance?

The clearance date for OCCLUDER, PATENT DUCTUS, ARTERIOSUS can be found in the official FDA records.

Who is the listed applicant for OCCLUDER, PATENT DUCTUS, ARTERIOSUS?

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

What is the FDA product code for OCCLUDER, PATENT DUCTUS, ARTERIOSUS?

The FDA product code for OCCLUDER, PATENT DUCTUS, ARTERIOSUS is MAE.

Related Clinical Trials

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.

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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.

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