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

EPIDURAL CATHETER TRAY

K Number: K840201 · Decision Mar 2, 1984
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
19
Review Days
43

Basic Information

Device Name
EPIDURAL CATHETER TRAY
K Number
K840201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3060
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
ARIES MEDICAL, INC.
Date Received
January 19, 1984
Decision Date
March 2, 1984
Product Code
MJL
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
MJL Eia, Blastomyces Dermatitidis

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