510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896629Substantially Equivalent

Nellcor Model N-2500 Anesthesia Safety Monitor

Nellcor, Inc., Hayward CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896629 is the FDA 510(k) clearance record for NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITOR, a class II device, cleared for Nellcor, Inc. on under FDA product code CBS (Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)). FDA records list 18 510(k) clearances for Nellcor, Inc., from to . As of , FDA records show no recalls naming K896629.

Clearance record

Decision date
Received
(82 days to decision)
Product code
CBS Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)
Regulation
21 CFR 868.1620
Device class
Class II
Review panel
Anesthesiology
Applicant
Nellcor, Inc. 25495 Whitesell St., Hayward CA
Third party review
No

Clearances, product code CBS

Trailing 12 months

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

FDA records show no clearances under product code CBS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CBS, 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