510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K921497Substantially Equivalent

Propaq Monitors, Modification

Protocol Systems, Inc., Beaverton OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921497 is the FDA 510(k) clearance record for PROPAQ MONITORS, MODIFICATION, a class II device, cleared for Protocol Systems, Inc. on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 15 510(k) clearances for Protocol Systems, Inc., from to . As of , FDA records show no recalls naming K921497.

Clearance record

Decision date
Received
(377 days to decision)
Product code
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Regulation
21 CFR 868.1400
Device class
Class II
Review panel
Anesthesiology
Applicant
Protocol Systems, Inc. 8500 SW Creekside Pl., Beaverton OR
510(k) summary
Summary
Third party review
No

Clearances, product code CCK

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