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

MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT

K Number: K050960 · Decision Jul 11, 2005
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
18
Applicant Total
22
Review Days
84

Basic Information

Device Name
MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT
K Number
K050960
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
862.1395
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WALLAC OY
Date Received
April 18, 2005
Decision Date
July 11, 2005
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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