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

MANOMETER

K Number: K122077 · Decision Jan 10, 2013
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
18
Review Days
178

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Basic Information

Device Name
MANOMETER
K Number
K122077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intersurgical, Inc.
Date Received
July 16, 2012
Decision Date
January 10, 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 Intersurgical, Inc.

K Number Device Name
K122075 DISPOSABLE GAS SAMPLING LINE WITH AND WITHOUT IN-LINE FILTER
K121026 FLO-GUARD BREATHING FILTER
K092451 INTERSURGICAL INTER-THERM BREATHING FILTER AND HEAT AND MOISTURE EXCHANGER, INTERSURGICAL INTER-GUARD BREATHING FILTER
K092129 INTERSURGICAL HEATED WIRE BREATHING SYSTEMS AND HUMIDIFICATION CHAMBERS, MODEL 2026,2026-CH, 2310, 2320, 2330
K092409 HYDRO-GUARD MINI BREATHING FILTER AND HEAT AND MOISTURE EXCHANGER AND AIR-GUARD CLEAR BREATHING FILTER
K032322 CLEAR-THERM MICRO HME, MODEL 1441
K024270 CLEAR-THERM 3 HMEF, CLEAR-THERM 3 WITH SUPERSET CATHETER MOUNT,CLEAR-THERM WITH FLEXIBLE CATHETER MOUNT,CLEAR-GUARD 3 F3
K990949 CLEAR-GUARD II, CLEAR-THERM HMEF, CLEAR-THERM HMEF W/ FLEXTUBE, CLEAR GUARD 11 W/ GAS MONITORING PORT
K983610 CLEAR-GUARD MIDI, CLEAR-GUARD MIDI W/FLEXTUBE, CLEAR-THERM MINI, CLEAR-THERM MINI W/FLEXTUBE, MODELS 1644,1644-T,1831,18
K984481 EXHALATION VALVE
Search all 18 clearances from Intersurgical, Inc. →