DeviceClearance

PE 501 PC-ECG MONITOR— 510(k) K992584

Substantially Equivalent

Nhe Corp.

FDA 510(k) clearance K992584 for PE 501 PC-ECG MONITOR, Substantially Equivalent on 2000-01-13. Applicant: Nhe Corp.. Device class: 2.

Clearance details

Applicant
Nhe Corp.
Product code
Code MWJ
Device class
Class 2
Regulation
21 CFR 870.2800
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Richmond, VA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MWJ

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Adverse events under product code MWJ

product code MWJ
Other
1
Total
1

Source: openFDA MAUDE database, through . 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.