510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K012451Substantially Equivalent

Propaq Encore Models 202, 204, 206; Propaq Cs Models 242, 244, 246

Welch Allyn Protocol, Inc., Beaverton OR / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K012451 is the FDA 510(k) clearance record for PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246, a class II device, cleared for Welch Allyn Protocol, Inc. on under FDA product code DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)). FDA records list 7 510(k) clearances for Welch Allyn Protocol, Inc., from to . As of , FDA records show no recalls naming K012451.

Clearance record

Decision date
Received
(19 days to decision)
Product code
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Regulation
21 CFR 870.2300
Device class
Class II
Review panel
Cardiovascular
Applicant
Welch Allyn Protocol, Inc. 8500 SW Creekside Pl., Beaverton OR
510(k) summary
Summary
Third party review
No

Clearances, product code DRT

Trailing 12 months
4 clearances under product code DRT in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260