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

DATEX-OHMEDA HMEF 750

K Number: K031653 · Decision Jun 20, 2003
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
40
Review Days
23

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Basic Information

Device Name
DATEX-OHMEDA HMEF 750
K Number
K031653
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda
Date Received
May 28, 2003
Decision Date
June 20, 2003
Product Code
CAH
Advisory Committee
Anesthesiology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
CAH Filter, Bacterial, Breathing-Circuit

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