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

DEKA SOLUTION ADMIN. SET DK 302-A

K Number: K843054 · Decision Sep 13, 1984
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
10
Review Days
41

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Basic Information

Device Name
DEKA SOLUTION ADMIN. SET DK 302-A
K Number
K843054
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Deka Research & Development Corp.
Date Received
August 3, 1984
Decision Date
September 13, 1984
Product Code
FPA
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
FPA Set, Administration, Intravascular

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