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

VITALERT 2000 VITAL SIGNS MONITOR

K Number: K882031 · Decision Jul 28, 1988
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
78
Review Days
73

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Basic Information

Device Name
VITALERT 2000 VITAL SIGNS MONITOR
K Number
K882031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Draeger Medical, Inc.
Date Received
May 16, 1988
Decision Date
July 28, 1988
Product Code
DXO
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
DXO Transducer, Pressure, Catheter Tip

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K041622 MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM
K040847 MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR
K033498 NARKOMED 6400, MODEL NM6400
K030624 MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM
K031400 FABIUS TIRO ANESTHESIA SYSTEM
K022031 NARKOMED MRI-2 ANESTHESIA SYSTEM, MODEL NM-MRI-2
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