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

DISPOSABLE PRESSURE MANOMETER

K Number: K022402 · Decision Aug 22, 2002
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
75
Review Days
30

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Basic Information

Device Name
DISPOSABLE PRESSURE MANOMETER
K Number
K022402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vital Signs, Inc.
Date Received
July 23, 2002
Decision Date
August 22, 2002
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 Vital Signs, Inc.

K Number Device Name
K112902 ENFLOW IV FLUID WARMER
K041309 IMASK TM
K030985 BREAS PV 10I CPAP SYSTEM, MODEL PV 10I
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
K984468 VITAL PEP
Search all 75 clearances from Vital Signs, Inc. →