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

NEIN ALLERGEN DISC IN VAST VENTREX TEST

K Number: K831554 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
261
Applicant Total
82
Review Days
26

Basic Information

Device Name
NEIN ALLERGEN DISC IN VAST VENTREX TEST
K Number
K831554
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5750
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
VENTREX LABORATORIES, INC.
Date Received
May 13, 1983
Decision Date
June 8, 1983
Product Code
DHB
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
DHB System, Test, Radioallergosorbent (Rast) Immunological

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Other Clearances by VENTREX LABORATORIES, INC.

K Number Device Name
K914554 SPECIFIC IGE EIA-TURBO ASSAY
K913833 VENTREX ALLERGEN DISC
K913434 VENTREX COATED TUBE INTACT PTH
K905612 VENTREX COATED TUBE IGE RADIOIMMUNOASSAY
K905636 VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
K905247 SHBG IRMA KIT
K904330 TURBO-RAST SPECIFIC IGE ASSAY
K903000 TURBO-RAST SPECIFIC IGE ASSAY
K897083 VENTRESIGN STREP A TEST
K895649 COATED TUBE HIGH SENSITIVITY TSH 200 UIU/ML STAN.
Search all 82 clearances from VENTREX LABORATORIES, INC. →