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

VITAL PEP

K Number: K984468 · Decision Jun 1, 1999
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
75
Review Days
167

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Basic Information

Device Name
VITAL PEP
K Number
K984468
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vital Signs, Inc.
Date Received
December 16, 1998
Decision Date
June 1, 1999
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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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
K022402 DISPOSABLE PRESSURE MANOMETER
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
Search all 75 clearances from Vital Signs, Inc. →