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

TIMOTHY ALLERGEN DISC

K Number: K862174 · Decision Aug 6, 1986
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
30
Review Days
58

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Basic Information

Device Name
TIMOTHY ALLERGEN DISC
K Number
K862174
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Immuno Nuclear Corp.
Date Received
June 9, 1986
Decision Date
August 6, 1986
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DGC), ordered by most recent decision date.

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Other Clearances by Immuno Nuclear Corp.

K Number Device Name
K863743 BIOTECH'S IGE IMMUNO RESPONSE TEST ISOTOPE UNIT
K863973 ELM ALLERGEN DISC
K863844 IMMUNO BIOTECH'S LAMB'S QUARTERS ALLERGEN DISC
K863123 IMMUNO BIOTECH MUGWART ALLERGEN DISC
K863098 MEADOW FESCUE ALLERGEN DISC
K862266 MAPLE ALLERGEN DISC
K862938 JUNE GRASS ALLERGEN DISC
K862176 RUSSIAN THISTLE ALLERGEN DISC
K862265 COTTONWOOD ALLERGEN DISC
K862939 ORCHARD GRASS ALLERGEN DISC
Search all 30 clearances from Immuno Nuclear Corp. →