PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246— 510(k) K012451

Name: FDA 510(k) clearance K012451
Creator: U.S. Food and Drug Administration
Published: 2001-08-20

Substantially Equivalent

Welch Allyn Protocol, Inc.

FDA 510(k) clearance K012451 for PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246, Substantially Equivalent on 2001-08-20. Applicant: Welch Allyn Protocol, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn Protocol, Inc.
Product code: Code DRT
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2001-08-01
Decision date: 2001-08-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Beaverton, OR, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRT

product code DRT

Death: 4
Total: 4

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.