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

AMBU HAND POWER SUCTION PUMP

K Number: K992902 · Decision Oct 25, 1999
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
33
Review Days
56

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Basic Information

Device Name
AMBU HAND POWER SUCTION PUMP
K Number
K992902
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ambu, Inc.
Date Received
August 30, 1999
Decision Date
October 25, 1999
Product Code
BSY
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
BSY Catheters, Suction, Tracheobronchial

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Other Clearances by Ambu, Inc.

K Number Device Name
K051529 AMBU NEUROLINE GROUND
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K042843 AMBU SPUR II INFANT AND PEDIATRIC SINGLE PATIENT USE RESUSCITATORS
K041734 AMBU DISPOSABLE ECG ELECTRODE
K040991 AMBU DISPOSABLE PRESSURE MANOMETER
K041026 AMBU BLUE SENSOR, MRX, ECG ELECTRODE PRODUCT #:MRX-00-S
K032278 AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE
K032421 AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE
K010583 AMBU GEL, HYDROGEL BURN DRESSING
K993278 AMBU NEONATE SILICONE RESUSCITATOR
Search all 33 clearances from Ambu, Inc. →