FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

VITAL PAK

K Number: K955417 · Decision Mar 8, 1996
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
75
Review Days
102

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Basic Information

Device Name
VITAL PAK
K Number
K955417
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
Vital Signs, Inc.
Date Received
November 27, 1995
Decision Date
March 8, 1996
Product Code
DXG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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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. →