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

AUTO DELFIA

K Number: K935047 · Decision May 23, 1994
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
37
Applicant Total
22
Review Days
214

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Basic Information

Device Name
AUTO DELFIA
K Number
K935047
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2560
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wallac OY
Date Received
October 21, 1993
Decision Date
May 23, 1994
Product Code
KHO
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
KHO Fluorometer, For Clinical Use

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Other Clearances by Wallac OY

K Number Device Name
DEN140010 PERKINELMER ENLITE NEONATAL TREC TEST SYSTEM
K131284 GSP NEONATAL BIOTINIDASE KIT
K100682 GSP NEONATAL 17A-OH-PROGESTERONE KIT MODEL: 3305-001U
K081922 AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
K071649 NEONATAL TOTAL GALACTOSE KIT; NEONTAL TOTAL GALACTOSE KIT, MODELS 3029-0010 AND 3029-110B
K070889 AUTODELFIA NEONATAL IRT L KIT, MODEL B022-112
K050709 RESOLVE HEMOGLOBIN KIT, JB-2 STAINING SYSTEM, MODELS FR-9120, FR-9400, FR-9360, FR-9367
K050960 MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT
K042424 DELFIA NEONATAL 17A-OH-PROGESTERONE KIT
K042425 AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
Search all 22 clearances from Wallac OY →