FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KALLESTAD HEP-2 CELL LINE SUBSTRATE

K Number: K810863 · Decision Apr 14, 1981
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
26
Applicant Total
92
Review Days
14

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Basic Information

Device Name
KALLESTAD HEP-2 CELL LINE SUBSTRATE
K Number
K810863
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5090
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
March 31, 1981
Decision Date
April 14, 1981
Product Code
DBM
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DBM Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control

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Other Clearances by Kallestad Laboratories, Inc.

K Number Device Name
K863681 PATHFINDER(TM) DIRECT ANTIGEN DETECTION SYSTEM
K862917 PATHFINDER ROTAVIRUS CHEMILUMINESCENT
K863682 PATHFINDER(TM) SPECIMEN COLLECTION KIT
K862743 PATHFINDER(TM) RESPIRATORY SYNCYTIAL VIRUS
K862313 KALLESTAD SM/RNP TEST REAGENT
K862710 KALLESTAD SSA/SSB ENA TEST REAGENTS
K855014 QUANTIMETRIC PLUS CALIBRATOR/CONTROL SET A
K855010 QUANTIMETRIC PLUS IGM REAGENT KIT
K855009 QUANTIMETRIC PLUS IGA REAGENT KIT
K855008 QUANTIMETRIC PLUS KAPPA REAGENT KIT
Search all 92 clearances from Kallestad Laboratories, Inc. →