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

END TIDAL CO2 SAMPLING CIRCUIT

K Number: K860659 · Decision Apr 17, 1986
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
87
Applicant Total
29
Review Days
52

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Basic Information

Device Name
END TIDAL CO2 SAMPLING CIRCUIT
K Number
K860659
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5975
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Life Design Systems, Inc.
Date Received
February 24, 1986
Decision Date
April 17, 1986
Product Code
BZO
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
BZO Set, Tubing And Support, Ventilator (W Harness)

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Other Clearances by Life Design Systems, Inc.

K Number Device Name
K913714 MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)
K885313 HUMIDI-FLEX TM
K893030 CHILD SIZE - FILTER FLEX (TM)
K892862 FLEX-CUP PERCUSSOR
K892221 PULMONARY RESUSCITATOR, MODIFICATION
K890011 OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING
K890108 MODIFIED CUSHION-FLEX(TM)
K884387 CUSHION FLEX(TM)
K884068 PULMANEX TM (NEO-NATAL SIZE)
K873179 HEATER WIRE BREATHING CIRCUIT
Search all 29 clearances from Life Design Systems, Inc. →