Atlas FDA

ALLERGENETICS ALLER-SPECIFIC IGE SERUM

FDA 510(k) clearance K842969 · decided 1984-08-28

Clearance details

K-number
K842969
Device name
ALLERGENETICS ALLER-SPECIFIC IGE SERUM
Applicant
Allergenetics
Decision
Substantially Equivalent
Date received
1984-07-30
Decision date
1984-08-28
Days to decision
29 days
Clearance type
Traditional
Product code
DGP
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VIDAS TOTAL IGE (IGE) ASSAY (K931224)Biomerieux Vitek, Inc.1993-05-20
IMMPULSE IGE ASSAY REAGENTS (K863327)Sclavo, Inc.1986-12-03
FIAX TOTAL IGE TEST KIT (K842749)Intl. Diagnostic Technology1984-08-28

Recalls involving this device

No recalls on record reference this clearance.