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

NEWBOURNS INFANT VENTILATOR

K Number: K802051 · Decision Oct 3, 1980
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
9
Review Days
39

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Basic Information

Device Name
NEWBOURNS INFANT VENTILATOR
K Number
K802051
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Bourns Medical Systems, Inc.
Date Received
August 25, 1980
Decision Date
October 3, 1980
Product Code
CBK
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
CBK Ventilator, Continuous, Facility Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.

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Other Clearances by Bourns Medical Systems, Inc.

K Number Device Name
K802118 BEAR 2 ADULT VOL. VENTILATOR
K801697 MODEL BP-200 INFANT PRESSURE VENTILATOR
K791186 MODEL BP-2000 TIME-CYCLED VENTILATOR
K790199 VENTILATOR MODEL BV-300 INFANT
K781760 HUMIDIFIERS, MODEL:LS-420 AND LS-460
K781485 PATIENT CIRCUIT MANIFOLD
K781515 MODEL LS-80 ADULT VENTILATION MONITOR
K781428 FLEXTUBES:9, 20, 26