510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K951246Substantially Equivalent - Subject to Tracking Reg.

Propaq Encore 200 Series Monitor with Neonatal Mode and Impedance Pneumography Options

Protocol Systems, Inc., Beaverton OR / Traditional, Substantially Equivalent - Subject to Tracking Reg.
FDA source (opens on fda.gov)

K951246 is the FDA 510(k) clearance record for PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS, a class II device, cleared for Protocol Systems, Inc. on under FDA product code FLS (Monitor, Apnea, Facility Use). FDA records list 15 510(k) clearances for Protocol Systems, Inc., from to . As of , FDA records show no recalls naming K951246.

Clearance record

Decision date
Received
(319 days to decision)
Product code
FLS Monitor, Apnea, Facility Use
Regulation
21 CFR 868.2377
Device class
Class II
Review panel
Anesthesiology
Applicant
Protocol Systems, Inc. 8500 SW Creekside Pl., Beaverton OR
Third party review
No

Clearances, product code FLS

Trailing 12 months

FDA records hold no clearances under product code FLS in the trailing twelve months.

FDA records show no clearances under product code FLS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FLS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260