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

PHADEZYM IGE PRIST TEST

K Number: K810507 · Decision Mar 20, 1981
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
129
Review Days
24

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Basic Information

Device Name
PHADEZYM IGE PRIST TEST
K Number
K810507
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Pharmacia, Inc.
Date Received
February 24, 1981
Decision Date
March 20, 1981
Product Code
DGC
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
DGC Ige, Antigen, Antiserum, Control

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Other Clearances by Pharmacia, Inc.

K Number Device Name
K974350 ALLERGAN IMMUNO CAP M4, M8, K70
K972364 UNICAP PHADIATOP
K972068 UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82
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
K951025 PISTON SYRINGE
K952025 ROBOCAP
Search all 129 clearances from Pharmacia, Inc. →