PNEUPAC RESUSCITATOR INSTANT ACTION SET— 510(k) K792451

Name: FDA 510(k) clearance K792451
Creator: U.S. Food and Drug Administration
Published: 1980-02-05

Substantially Equivalent

Pneupac , Ltd.

FDA 510(k) clearance K792451 for PNEUPAC RESUSCITATOR INSTANT ACTION SET, Substantially Equivalent on 1980-02-05. Applicant: Pneupac , Ltd.. Device class: 2.

Clearance details

Applicant: Pneupac , Ltd.
Product code: Code DRM
Device class: Class 2
Regulation: 21 CFR 870.5200
Advisory panel: Cardiovascular
Date received: 1979-12-03
Decision date: 1980-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K221700 — AutoPulse NXT Resuscitation System2023-03-09
K211289 — RMU-2000 Automated Chest Compression System2021-11-09
K173553 — LUCAS 3 Chest Compression System2018-02-08
K161768 — LUCAS 3 Chest Compression System2016-11-09
K153628 — ROSC-U Mini Chest Compressor (RMCC)2016-01-30

More clearances from Pneupac , Ltd.

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K040090 — COMPPAC 200HD; CS12 POWER SUPPLY (AIRCRAFT/VECHILE); PS11 POWER SUPPLY (MAINS)2004-05-27
K030803 — PARAPAC 200D TRANSPORT, MODEL V200D2003-09-29
K021841 — COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER2003-07-17
K020899 — PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200D2002-12-13
K960515 — PARAPAC1996-10-10

Adverse events under product code DRM

product code DRM

Death: 82
Injury: 126
Malfunction: 4,539
Total: 4,747

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.