510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896652Substantially Equivalent

Capnomac Ultima(tm) Anesthesia Monitor

Datex Division Instrumentarium Corp., Helsinki, Finland, FI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896652 is the FDA 510(k) clearance record for CAPNOMAC ULTIMA(TM) ANESTHESIA MONITOR, a class II device, cleared for Datex Division Instrumentarium Corp. on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 55 510(k) clearances for Datex Division Instrumentarium Corp., from to . As of , FDA records show no recalls naming K896652.

Clearance record

Decision date
Received
(285 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
Datex Division Instrumentarium Corp. P.O. Box 446, Helsinki, Finland, FI
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