FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

THERMOVENT 600, 1200, T, 02

K Number: K874597 · Decision Jan 19, 1988
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
20
Review Days
71

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Basic Information

Device Name
THERMOVENT 600, 1200, T, 02
K Number
K874597
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Portex, Inc.
Date Received
November 9, 1987
Decision Date
January 19, 1988
Product Code
BYD
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
BYD Condenser, Heat And Moisture (Artificial Nose)

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K023793 1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
K014115 1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX
K014073 HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE
K873992 LARYNGECTOMY TUBE
K862167 MINI-TRACH KIT
K842456 JET VENTILATION ADAPTOR
K833908 IRRI-CATH
K840015 SWIVEL ADAPTOR W/ALARM PORT
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