PARAPAC 200D TRANSPORT, MODEL V200D— 510(k) K030803

Name: FDA 510(k) clearance K030803
Creator: U.S. Food and Drug Administration
Published: 2003-09-29

Substantially Equivalent

Pneupac , Ltd.

FDA 510(k) clearance K030803 for PARAPAC 200D TRANSPORT, MODEL V200D, Substantially Equivalent on 2003-09-29. Applicant: Pneupac , Ltd.. Device class: 2.

Clearance details

Applicant: Pneupac , Ltd.
Product code: Code BTL
Device class: Class 2
Regulation: 21 CFR 868.5925
Advisory panel: Anesthesiology
Date received: 2003-03-13
Decision date: 2003-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waukesha, WI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BTL

product code BTL

Death: 8
Malfunction: 3,256
Other: 1
Total: 3,265

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.