FDA 510(k) FDA class 1 Substantially Equivalent 🇫🇮 Finland

AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT

K Number: K081922 · Decision Apr 16, 2009
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
18
Applicant Total
22
Review Days
283

Basic Information

Device Name
AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
K Number
K081922
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1395
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WALLAC OY
Date Received
July 7, 2008
Decision Date
April 16, 2009
Product Code
JLX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JLX Radioimmunoassay, 17-Hydroxyprogesterone

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