Haftungsausschluss: Diese Website bündelt öffentlich verfügbare Daten aus offiziellen Quellen wie FDA, ClinicalTrials.gov, PubMed und SEC EDGAR nur zur allgemeinen Information. Sie stellt keine medizinische Beratung, Diagnose, Behandlungsempfehlung oder Anlageberatung dar.

FDA-PMA

Combination compression/decompression manual chest pump with impedance respiratory valve

PMA-Nummer: P110024 · 2026-08-27

AntragstellerZOLL Medical Corporation
Entscheidungsdatum2026-08-27
PMA-NummerP110024
ProduktcodePIZ
GeräteklasseKlasse 3
Medizinische FachrichtungU
BeratungsausschussCV

Produktübersicht

Combination compression/decompression manual chest pump with impedance respiratory valve is the device name listed in this FDA 510(k) record. The listed applicant is ZOLL Medical Corporation. It received FDA 510(k) clearance on 2026-08-27. The device is classified under product code PIZ. It was reviewed by the CV advisory panel.

Häufig gestellte Fragen

What is the Combination compression/decompression manual chest pump with impedance respiratory valve?

Combination compression/decompression manual chest pump with impedance respiratory valve is a medical device that received FDA 510(k) clearance on 2026-08-27. The listed applicant is ZOLL Medical Corporation.

When did Combination compression/decompression manual chest pump with impedance respiratory valve receive FDA 510(k) clearance?

The clearance date for Combination compression/decompression manual chest pump with impedance respiratory valve can be found in the official FDA records.

Who is the listed applicant for Combination compression/decompression manual chest pump with impedance respiratory valve?

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

What is the FDA product code for Combination compression/decompression manual chest pump with impedance respiratory valve?

The FDA product code for Combination compression/decompression manual chest pump with impedance respiratory valve is PIZ.

Zugehörige klinische Studien

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Offizielle Quelle

In der FDA-Datenbank anzeigen →

Daten aus der FDA Open API. Für die aktuellsten und verbindlichen Informationen konsultieren Sie bitte stets den offiziellen Datensatz.

↑