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

SUZANNE

K Number: K990565 · Decision Aug 18, 1999
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
42
Review Days
177

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Basic Information

Device Name
SUZANNE
K Number
K990565
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nellcor Puritan Bennett, Inc.
Date Received
February 22, 1999
Decision Date
August 18, 1999
Product Code
MNR
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
MNR Ventilatory Effort Recorder

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K051271 OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR
K052186 NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-P
K051352 OXIMAX NPB-40 HANDHELD PULSE OXIMETER
K050072 GOODKNIGHT 425ST
K033973 OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR
K030787 SHILEY FLEXTRA TRACHEOSTOMY TUBE
K030930 OXIMAX SOFTCARE SENSORS, MODELS SC-A, SC-PR, SC-NEO, SC-N
K023494 NELLCOR INDGO MANUAL RESUSCITATOR
Search all 42 clearances from Nellcor Puritan Bennett, Inc. →