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

KALLESTAD QUANTITOPE LOW LEVEL IGE REAG

K Number: K811545 · Decision Jun 24, 1981
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
92
Review Days
23

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Basic Information

Device Name
KALLESTAD QUANTITOPE LOW LEVEL IGE REAG
K Number
K811545
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
June 1, 1981
Decision Date
June 24, 1981
Product Code
DGC
Advisory Committee
Immunology
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
DGC Ige, Antigen, Antiserum, 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. →