FDA 510(k) Substantially Equivalent 🇺🇸 United States

LEECO DIG-QUANT DIAG. TEST KIT

K Number: K830785 · Decision Apr 8, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
49
Review Days
28

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Basic Information

Device Name
LEECO DIG-QUANT DIAG. TEST KIT
K Number
K830785
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Leeco Diagnostics, Inc.
Date Received
March 11, 1983
Decision Date
April 8, 1983
Advisory Committee
Unknown
Review Advisory Committee
CH
Third Party
N

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K891096 VIS-DISK HCG (EIA) JPL-041M
K883269 PRL-QUANT
K880577 CONCEP-7-BHCG
K880069 LEECO PREGNASTICK (EIA) CATALOG #003
K870259 VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044
K864170 LEECO VIS-CUBE STREP A (EIA)
K863999 VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042
Search all 49 clearances from Leeco Diagnostics, Inc. →