510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K992584Substantially Equivalent

Pe 501 Pc-ECG Monitor

Nhe Corp., Richmond VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992584 is the FDA 510(k) clearance record for PE 501 PC-ECG MONITOR, a class II device, cleared for Nhe Corp. on under FDA product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)). FDA records list one 510(k) clearance for Nhe Corp. As of , FDA records show no recalls naming K992584.

Clearance record

Decision date
Received
(164 days to decision)
Product code
MWJ Electrocardiograph, Ambulatory (Without Analysis)
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Nhe Corp. 7100 Fernwood Ave., Richmond VA
510(k) summary
Summary
Third party review
No

Clearances, product code MWJ

Trailing 12 months
5 clearances under product code MWJ in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MWJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20260
August 20261
September 20262
October 20260