510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K851001Substantially Equivalent

Series 7000 End Tidal CO2 Monitoring System

Marquette Electronics, Inc., Milwaukee WI / Traditional, Substantially Equivalent

K851001 is the FDA 510(k) clearance record for SERIES 7000 END TIDAL CO2 MONITORING SYSTEM, a class II device, cleared for Marquette Electronics, Inc. on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 82 510(k) clearances for Marquette Electronics, Inc., from to . As of , FDA records show no recalls naming K851001.

Clearance record

Decision date
Received
(62 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
Marquette Electronics, Inc. 8200 W. Tower Ave., Milwaukee WI
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