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FDA PMA

Combination compression/decompression manual chest pump with impedance respiratory valve

PMA Number: P110024 · 2026-08-27

ApplicantZOLL Medical Corporation
Decision Date2026-08-27
PMA NumberP110024
Product CodePIZ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

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.

Frequently Asked Questions

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.

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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