FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

DELFIA DIGOXIN KIT

K Number: K924594 · Decision Dec 17, 1992
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
84
Applicant Total
22
Review Days
98

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DELFIA DIGOXIN KIT
K Number
K924594
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3320
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Wallac OY
Date Received
September 10, 1992
Decision Date
December 17, 1992
Product Code
KXT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
KXT Enzyme Immunoassay, Digoxin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KXT), ordered by most recent decision date.

View all

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 →