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

DRAGER OXYLOG 2000

K Number: K984577 · Decision Jan 22, 1999
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
20
Review Days
30

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DRAGER OXYLOG 2000
K Number
K984577
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Drager, Inc.
Date Received
December 23, 1998
Decision Date
January 22, 1999
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.

View all

Other Clearances by Drager, Inc.

K Number Device Name
K992608 ATC OPTION FOR EVITA 2 DURA AND EVITA 4
K983219 NEOFLOW OPTION MODEL NUMBERS 8413563, 8411900
K982789 MEDICAL AIR COMPRESSOR, MODEL # 8413419
K980642 EVITA 4 (8411900)
K974176 BABYLOG 8000 PLUS
K971198 BABYTHERM 8004 BABYTHERM 8010
K970165 EVITA 2 DURA
K954204 DRAGER INCUBATOR 8000 IC
K961687 EVITA 4
K950853 OPTIONAL DISPLAY AND SOFTWARE FOR DRAGER VENTILATORS
Search all 20 clearances from Drager, Inc. →