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

PRESSURE MANOMETER

K Number: K110119 · Decision Jun 10, 2011
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
7
Review Days
143

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Basic Information

Device Name
PRESSURE MANOMETER
K Number
K110119
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neoforce Group, Inc.
Date Received
January 18, 2011
Decision Date
June 10, 2011
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)

Similar 510(k) Clearances

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Other Clearances by Neoforce Group, Inc.

K Number Device Name
K103833 NEOPIP PATIENT CIRCUIT WITH PEEP
K102649 NEOPOP INFANT RESUSCITATOR WITH FLOW METER
K092085 ISPIRA RESUSCITATION UNIT
K072021 NEOPIP INFANT RESUSCITATOR
K070416 NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP
K061280 V-2200 INFANT INCUBATOR