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

AMBU DISPOSABLE PRESSURE MANOMETER

K Number: K040991 · Decision Jul 22, 2004
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
33
Review Days
97

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Basic Information

Device Name
AMBU DISPOSABLE PRESSURE MANOMETER
K Number
K040991
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ambu, Inc.
Date Received
April 16, 2004
Decision Date
July 22, 2004
Product Code
CAP
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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Other Clearances by Ambu, Inc.

K Number Device Name
K051529 AMBU NEUROLINE GROUND
K042682 AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR
K042843 AMBU SPUR II INFANT AND PEDIATRIC SINGLE PATIENT USE RESUSCITATORS
K041734 AMBU DISPOSABLE ECG ELECTRODE
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
K992902 AMBU HAND POWER SUCTION PUMP
Search all 33 clearances from Ambu, Inc. →