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

AMBU SUCTION BOOSTER

K Number: K790035 · Decision Mar 23, 1979
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
2
Applicant Total
19
Review Days
77

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Basic Information

Device Name
AMBU SUCTION BOOSTER
K Number
K790035
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Narco Air-Shields
Date Received
January 5, 1979
Decision Date
March 23, 1979
Product Code
CBC
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
CBC Bottle, Collection And Trap, Breathing System (Uncalibrated)

Similar 510(k) Clearances

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Other Clearances by Narco Air-Shields

K Number Device Name
K820114 SYSTEM V.HEART RATE/RESPIR. RATE MONIT.
K810953 MODEL 533 PHOTOTHERAPY UNIT
K810474 PROBE COVER
K802800 NARCO AIR-SHEILDS SYS. 100 MONITOR SYS
K802126 ISOLETTE INCUBATOR C-100
K792592 AMBU UNIVERSAL SUCTION PUMP
K792499 AMBU PAEDI ANAESTHESIA SYSTEM
K792117 AIR-SHIELDS HEART RATE MONITOR
K792118 AIR-SHIELDS RESUSCITATORS
K790552 AS7 & AS8 MONITORS
Search all 19 clearances from Narco Air-Shields →