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

GIO DIGITAL PRESSURE GUAGES

K Number: K122627 · Decision Aug 22, 2013
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
7
Review Days
359

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Basic Information

Device Name
GIO DIGITAL PRESSURE GUAGES
K Number
K122627
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Galemed Corp.
Date Received
August 28, 2012
Decision Date
August 22, 2013
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

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

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Other Clearances by Galemed Corp.

K Number Device Name
K132679 AF VIRAL/BACTERIAL FILTER, BF VIRAL/BACTERIAL FILTER
K133957 DISPOSABLE ADJUSTABLE PEEP VALVE MR CONDITIONAL USE
K082092 DISPO-BAG MANUAL RESUSCITATOR, DISPOSABLE ADJUSTABLE PEEP VALVE, DISPOSABLE FIXED PEEP VALVE
K072755 GALEMED CPAP MASK
K022124 GALEMED PEAK FLOW METER, MODELS 3751/3752
K021742 GALEMED NEB-EASY NEBULIZER