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

DIVAN ANESTHESIA VENTILATOR

K Number: K980208 · Decision Aug 4, 1998
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
78
Review Days
196

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Basic Information

Device Name
DIVAN ANESTHESIA VENTILATOR
K Number
K980208
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Draeger Medical, Inc.
Date Received
January 20, 1998
Decision Date
August 4, 1998
Product Code
CBK
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
CBK Ventilator, Continuous, Facility Use

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Other Clearances by Draeger Medical, Inc.

K Number Device Name
K042607 PRIMUS US
K042419 FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEM
K042276 D-VAPOR
K042086 FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM
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
Search all 78 clearances from Draeger Medical, Inc. →