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FDA PMA

diaphragmatic/phrenic nerve laparoscopically-implanted stimulator

PMA Number: P200018 · 2023-03-31

Decision Date2023-03-31
PMA NumberP200018
Product CodeOIR
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeAN

Device Summary

diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Synapse Biomedical, Inc.. It received FDA 510(k) clearance on 2023-03-31. The device is classified under product code OIR. It was reviewed by the AN advisory panel.

Frequently Asked Questions

What is the diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?

diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is a medical device that received FDA 510(k) clearance on 2023-03-31. The listed applicant is Synapse Biomedical, Inc..

When did diaphragmatic/phrenic nerve laparoscopically-implanted stimulator receive FDA 510(k) clearance?

The clearance date for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator can be found in the official FDA records.

Who is the listed applicant for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?

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

What is the FDA product code for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?

The FDA product code for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is OIR.

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.

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.

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