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

I.V. SENTINEL

K Number: K821823 · Decision Aug 16, 1982
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
38
Applicant Total
20
Review Days
55

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Basic Information

Device Name
I.V. SENTINEL
K Number
K821823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2420
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
The John Bunn Co.
Date Received
June 22, 1982
Decision Date
August 16, 1982
Product Code
FLN
Advisory Committee
General Hospital
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
FLN Monitor, Electric For Gravity Flow Infusion Systems

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K855208 BUNN LITE OXYGEN CONCENTRATOR
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