FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITOR

K Number: K896629 · Decision Feb 12, 1990
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
16
Applicant Total
18
Review Days
82

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Basic Information

Device Name
NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITOR
K Number
K896629
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1620
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Nellcor, Inc.
Date Received
November 22, 1989
Decision Date
February 12, 1990
Product Code
CBS
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CBS Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)

Similar 510(k) Clearances

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Other Clearances by Nellcor, Inc.

K Number Device Name
K953472 NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR
K952316 NELLCOR SYMPHONY N-3000 PULSE OXIMETER
K952222 NELLCOR N-20PA PORTABLE PULSE OXIMETER
K942347 NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000
K945947 NELLCOR SYMPHONY(TM) N-3100 BLOOD PRESSURE MONITOR AND CONNECTED TO THE NELLCOR SYMPHONY(TM) N-3000 PULSE OXIMETER
K944760 DURA-Y OXYGEN TRANSDUCER, EAR CLIP
K944400 PEDI-CAP
K915494 NELLCOR STAT-CAP AIRWAY CO2 INDICATOR, MODEL N-60
K915699 NELLCOR PORTABLE PULSE OXIMETER MODEL N-20
K913695 NELLCOR(R) N-180 PULSE OXIMETER
Search all 18 clearances from Nellcor, Inc. →