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

VENTREX DATA REDUCTION & QUAL. CONTR. SY

K Number: K812357 · Decision Sep 1, 1981
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
82
Review Days
12

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Basic Information

Device Name
VENTREX DATA REDUCTION & QUAL. CONTR. SY
K Number
K812357
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Ventrex Laboratories, Inc.
Date Received
August 20, 1981
Decision Date
September 1, 1981
Product Code
JPK
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JPK Mixture, Hematology Quality Control

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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
K895648 COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.
Search all 82 clearances from Ventrex Laboratories, Inc. →