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

PHADEBAS IGG RAST TEST

K Number: K810694 · Decision Jul 23, 1981
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
75
Applicant Total
129
Review Days
129

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Basic Information

Device Name
PHADEBAS IGG RAST TEST
K Number
K810694
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Pharmacia, Inc.
Date Received
March 16, 1981
Decision Date
July 23, 1981
Product Code
DEW
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
DEW Igg, Antigen, Antiserum, Control

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K970420 MASTERCAP AM 5.0/MASTERCAP RM 5.0
K964152 UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH
K962274 UNICAP 100
K941993 PHARMACIA CAP SYSTEM PHADIATOP FEIA
K954337 GENOTROPIN MIXER
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K952025 ROBOCAP
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